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Test Definition
Test Definition
Test Test Description To Print Test Code Unit QC Cost Result Type Round off Numeric Result Type Assay Content Microbial Retest Test for Water/LOD
# 100 0 Character N N N
# 20 mesh 0 Character N N N
#200 mesh 0 Character N N N
#60 mesh 0 Character N N N
% Single Maximum unknown impurity: 0 Character N N N
% Total unknown impurity: 0 Character N N N
(a) By Light Obscuration Particle Count Test ≥ 10µm 0 Character N N N N
(a) Sulbactam 0 Character N N N N
(b) By Light Obscuration Particle Count Test ≥ 25µm 0 Character N N N N
(b) Cefoperazone 0 Character N N N N
(on anhydrous basis) 0 Character N N N
(on as is basis) 0 Character N N N
*Ink lifting test 0 Character N N N
-RRT 0.86 0 Character N N N
-RRT 1.27 0 Character N N N
-RRT 1.39 0 Character N N N
-RRT > 2.0 0 Character N N N
. p- toluene sulphonamide 0 Character N N N
1) Lidocaine Hydrochloride BP: 10.0 mg/mL 0 Character N N N
1)Diethylene glycol 0 Character N N N
1,4 Dioxane 0 Character N N N N
1-vinylpyrrolidin-2-one 0 Character N N Y
12- hydroxyl stearic acid 0 Character N N N
12-oxosteric acid 0 Character N N N
2) Ethylene glycol 0 Character N N N
2) Sodium Chloride BP: 7.0 mg/mL 0 Character N N N
2,6 Dimethylaniline 0 Character N N N
2- Ethylhexanoic acid by GC 0 Character N N N
2-Hydroxy-2-methyl-proplophenone (2-HMP) 0 Character N N N N
2-methylbut -2-ene 0 Character N N N
2-Propanol 0 Character N N N
2-Pyrrolidone 0 Character N N N
28.5 ml to 31.5 ml 0 Character N N N
2D Code 0 Character N N N
3) Methyl Paraben BP: 1.0 mg/mL 0 Character N N N
45MIC x 300MM LDPE SHRINK FILM 0 Character N N N
5 Ply C/Box 410X280X215 Oflox -D 0 Character N N N
5-Benzyl-3,6-dioxo-2-piperazineacetic acid 0 Character N N N
6- Bromopenicillanic Acid Sulphone 0 Character N N N
7-Aminocephalosporanic acid (if present) 0 Character N N N
A Assay (Initial): by HPLC Each 5 ml reconstituted suspension contains:Cefixime IP (as Trihydrate) equivalent to Anhydrous Cefixime 100 mg. 0 Character N N N
A NLT 75% (D) i.e 80 % of the stated amount of Cefixime released in 45 min. 0 Character N N N
A ) Assay (in %) (Each vial contains: Ceftriaxone Sodium Eq. to Ceftriaxone 0 Numeric Range N N N
A ) By chemically 0 Character N N N
A) 0 Character N N N
A) A)When sample is strongly heated becomes pale yellow, the colour discharge on cooling. 0 Character N N N
A) Assay (Initial): by HPLC 0 Character N N N
A) Assay (Initial): by HPLC Each 5 ml reconstituted suspension contains:Cefixime IP (as Trihydrate) equivalent to Anhydrous Cefixime 100 mg. 0 Character N N N
A) By IR 0 Character N N N
A) Cefixime 0 Character N N N
A) Cefixime released in 45 min. 0 Character N N N
a) 2.5 ml marking 0 Character N N N
A) Assay (Initial): Each 5 ml reconstituted suspension contains: Cefixime Trihydrate IP equivalent to Cefixime anhydrous 50 mg 0 Character N N N
A) Assay (Initial): Cephalexin IP equivalent to anhydrous Cephalexin 125 mg. 0 Character N N N
A) Assay (Initial):Each 5 ml of the reconstituted suspension contains:Cefixime IP as Trihydrate equivalent to anhydrous Cefixime 100 mg. 0 Character N N N
A) Average net volume 0 Character N N N
A) By Banzoates 0 Character N N N
A) By Colour test 0 Character N N N
A) By Freezing point 0 Character N N N
A) By HPLC 0 Character N N N
A) By IR 0 Character N N N
A) By IR (method I) 0 Character N N N
A) By Magnesium test 0 Character N N N
A) By microscopy 0 Character N N N
A) By Relative density 0 Character N N N
A) By Specific rotation 0 Character N N N
A) By TLC 0 Character N N N
A) By UV 0 Character N N N
A) By visual inspection 0 Character N N N
A) By visual test 0 Character N N N
A) Chloride Test 0 Character N N N
A) Clarity with water 0 Character N N N
A) Escherichia coli 0 Character N N N
A) Freezing point 0 Character N N N
A) I- Indication for a polymeric compound 0 Character N N N
a) Less than 0.5 % Particles should retain on #60 mesh ASTM (250µm) 0 Character N N N
A) Melting point 0 Character N N N
A) NLT 50 % (Q) i.e 55 % of the labeled amount of cefuroxime released in 15 min. 0 Character N N N
A) Sulbactam (activity) 0 Character N N N N
A) Total aerobic microbial count 0 Character N N N
A)1 For Cefixime % Single Maximum Impurity: 0 Character N N N
A)2 For Cefixime % Total Impurities: 25 250 Character Y Y Y
A)Assay (Initial): by HPLC Cefixime USP (as Trihydrate) equivalent to Anhydrous Cefixime 50 mg. 0 Character N N N
A)Assay (Initial): by HPLC Each 5 ml reconstituted suspension contains: Cefixime Trihydrate IP equivalent to Cefixime anhydrous 50 mg. 0 Character N N N
A)Assay (Initial): by HPLCEach 5 ml reconstituted suspension contains: Ofloxacin IP 50 mg: 0 Character N N N
A)Assay (Initial): Cefpodoxime Proxetil IP equivalent to Cefpodoxime 50 mg.. 0 Character N N N
A)Assay by HPLCEach 5 ml of the reconstituted suspension contains:Cefpodoxime Proxetil IP equivalent to Cefpodoxime 50 mg. 0 Character N N N
A)Assay by weight: Ceftriaxone USP on Anhydrous Basis 0 Character N N N
A)Average net volume 0 Character N N N
A)By Chemical 0 Character N N N
a)NLT 60 % (Q) i.e 65 % of the labeled amount of cefuroxime released in 15 min. 0 Character N N N
A)NLT 90% of L.C the stated amount of Cefixime released in 45 min. 0 Character N N N
A-. Stearic acid 0 Character N N N
A. Benzene 0 Character N N N
A. II –Distinction from locust Bean Gum 0 Character N N N
A. Thiazolylacetyl glycine oxime 0 Character N N N
A.) Glass Grain Test 0 Character N N N
A1) For Tazobactam % Single Maximum unknown impurity: 0 Character N N N
A2) For Tazobactam % Total unknown impurity: 0 Character N N N
Absorbance 0 Character N N N
Acetic Acid 0 Character N N N
Acetone 0 Character N N N
Acetone(%w/w) By GC 0 Character N N N
Acetonitrile 0 Character N N N
Acetyl value 0 Character N N N
Acid value of the fatty acids 0 Character N N N
Acid insoluble substances 0 Character N N N
Acid soluble Substances 0 Character N N N
Acid Value 0 Character N N N
acid1 0 Character N N N
Acidity 0 Character N N N
Acidity or Alkalinity 0 Character N N N
Acidity or Alkalinity (pH ) 0 Character N N N
Acidity or alkalinity (B.)Methyl orange indicator 0 Character N N N
Acidity or alkalinity( A.)BPR indicator 0 Character N N N
Adhesive 0 Character N N N
Adhesive Coating 0 Character N N N
Adhesive Gsm 0 Character N N N
Adhesive layer GSM 0 Character N N N
Adhesive Test 0 Character N N N
Adsorption Capacity 0 Character N N N
Aldehydes 0 Character N N Y
Aldehydes and Ketones 0 Character N N N
Alignment 0 Character N N N
Alkaline impurities 0 Character N N N
Alkalinity 0 Character N N N
All other Impurities 0 Character N N N
Alu foil gsm* 0 Character N N N
Alu foil Thickness 0 Character N N N
Aluminium 0 Character N N N
Aluminium (Chemical Method) 0 Character N N N
Aluminium GSM 0 Character N N N
Aluminium Thickness(mm) 0 Character N N N
Aluminum (as AL) 0 Character N N N
Aluminum, calcium & related elements 0 Character N N N
Ammonia Compounds 0 Character N N N
Ammonium 0 Character N N N
Amoxicillin Related Compound A 0 Character N N N
Anhydrous Di-sodium hydrogen 0 Character N N N
Antimony 0 Character N N N
Any Individual Impurity 0 Character N N N
Any Individual unspecified impurity 0 Character N N N
Any maximum impurity 0 Character N N N
Any other highest unknown impurity 0 Character N N N
Any other Impurity 0 Character N N N
Any Other Individual Impurity 0 Character N N N
any other of fatty acid 0 Character N N N
Any other secondary impurity 0 Character N N N
Any Unspecified degradation product 0 Character N N N
Appearance 0 Character N N N
Appearance After Constitution 0 Character N N N
Appearance of Content 0 Character N N N
Appearance of solution 0 Character N N N
Appearance of solution (A.)Clarity of solution 0 Character N N N
Appearance of solution (B.)Colour of solution 0 Character N N N
Appearance of solution (Clarity and colour of solution) 0 Character N N N
Appearance of solution of the fatty acid 0 Character N N N
Apperance of solution (1.2 % w/v solution in water) 0 Character N N N
AQL 0 Character N N N
Arachidic acid 0 Character N N N
Arsenic 0 Character N N N
Arsenic (as AS ) 0 Character N N N
Arsenic (as As) 0 Character N N N
Arsenic Test(µg) 0 Character N N N
Artwork code 0 Character N N N
Ash 0 Character N N N
Assay 0 Character N N N
Assay Potency (HPLC) withdrawable basis 0 Character N N N N
Assay ( In House ) 0 Character N N N
Assay ( on ignite basis ) 0 Character N N N
Assay (By Potentiometry) 0 Character N N N
Assay (mg per vial) Each vial contains:Cefoperazone Sodium IPEq. to Cefoperazone 0 Character N N N
Assay ( Bacterial count ) 0 Character N N N
Assay ( By GC) 0 Character N N N
Assay ( on anhydrous basis ) 0 Character N N N
Assay (% Lable claim) Each vial containes: Ceftriaxone Sodium IP eq. to Ceftriaxone % 0 Numeric Range N N N
Assay (% w/w) by HPLC (as Tazobactam on anhydrous basis) % 0 Numeric Range N N N
Assay (% w/w) by HPLC (on anhydrous basis and acetone free basis) % 0 Character N N N
Assay (% w/w) by HPLC (on anhydrous basis) 0 Character N N N
Assay (% w/w) by HPLC (on as is basis) 0 Character Y N N
Assay (% w/w) by HPLC* 0 Character N N N
Assay (%w/w, on anhydrous basis, as Enmetazobactam ( By HPLC) 0 Character N N N
Assay (After 7th day) by HPLC Each 5 ml of the reconstituted suspension contains:Cefpodoxime Proxetil IP equivalent toCefpodoxime 100 mg. 0 Character N N N
Assay (By HPLC %(on dried and sodium carbonate-free basis) 0 Character N N N N
Assay (by HPLC µg/mg of Cefpodoxime on anhydrous basis) 0 Character N N N
Assay (By HPLC) 0 Character N N N
Assay (By HPLC) (Cefixime on anhydrous basis) 0 Character N N N
Assay (By HPLC) (on anhydrous basis) 0 Character N N N
Assay (By HPLC) Content of Ceftazidime on as is basis 0 Character N N N N
Assay (By HPLC) On as is basis Avibactam content 0 Character N N N N
Assay (By Ion chromatography) Content of Sodium chloride 0 Character N N N N
Assay (By titration) 0 Character N N N
Assay (By Titrimetry) On dried basis 0 Character N N N
Assay (By Titrimetry)Magnesium(on dried basis) 0 Character N N N
Assay (g/vial)Each vial contains:Ceftriaxone Sodium USP eq. to Ceftriaxone 0 Character N N N
Assay (mg per vial ) Chaque flacon contient:Ceftriaxone Sodium BP Eq. to Ceftriaxone . 0 Character N N N
Assay (mg per vial) Each vial contains: Cefuroxime Sodium IP eq. to Cefuroxime 0 Character N N N
Assay (mg per vial)Each vial contains:Ceftriaxone Sodium BP Equivalent to Ceftriaxone 1 g 0 Character N N N
Assay (mg per vial)Each vial contains:Ceftriaxone Sodium BP Equivalent to Ceftriaxone 500 mg 0 Character N N N
Assay (mg/vial)Each vial contains:Ceftriaxone Sodium IP (Sterile)eq. to Ceftriaxone 250 mg 0 Character N N N
Assay (On Anhydrous basis) 0 Character N N N N
Assay (on anhydrous basis): By potentiometry. 0 Character N N N
Assay (on ignite basis) 0 Character N N N
Assay (on the anhydrous basis) 0 Character N N N
Assay (on the dried basis) 0 Character N N N
Assay : by HPLC Each film coated tablet contains: 0 Character N N N
ASSAY : By Titrimetry 0 Character N N N
Assay By AAS (%w/w) (Content of Galactomannans) 0 Character N N N
Assay By GC 0 Numeric Range N N N
Assay by HPLC 0 Character N N N N
Assay By HPLC (in µg/mg, on anhydrous basis) 0 Character N N N
Assay by HPLC (on dried basis) 0 Character N N N
Assay by tirimetry 0 Character N N N
Assay by Titration ( on dried basis) 0 Character N N N
Assay of Ceftazidime ( By HPLC , on as is basis) 0 Character N N N
Assay of Ciprofloxacin 0 Character N N N
Assay of Dexamethasone 0 Character N N N
ASSAY OF Si02 (%) Calculated on the ignite basis 0 Character N N N
Assay on 14th day of reconstitution 0 Character N N N
Assay on dried basis % w/w 0 Character N N N
Assay pyruvoyl groups ( on dried basis ) 0 Character N N N
Assay(w/w) by HPLC (ceftriaxone on anhydrous basis) 0 Character N N N
Assay: By HPLC 0 Character N N N
Assay: by HPLC Each 5 ml of the reconstituted suspension contains: Cefadroxil IP Equivalent to anhydrous Cefadroxil 125 mg. 0 Character N N N
Assay: by HPLC, Each 5 ml of the reconstituted suspension contains: Cefuroxime Axetil USP equivalent to Cefuroxime 125 mg: 0 Character N N N
Assay: By Titrimetry: 0 Character N N N
Assay: By titrimetry: calculated on the dried basis. 0 Character N N N
Assay: By Ultraviolet and visible absorption spectrophotometry: calculated with reference to the dried substance. 0 Character N N N
Assay: Each vial contains Cefotaxime sodium (sterile) USP eq. to Cefotaxime 1g 0 Character N N N
Assay: Each vial contains Cefotaxime sodium (sterile) USP eq. to Cefotaxime 500 mg 0 Character N N N
Assay: Ratio of Alkyl components. (By: HPLC.) n-C12H25 homolog 0 Character N N N
Assay: Ratio of Alkyl components. Total amounts of the n-C12H25 & n-C14H29 homolog. 0 Character N N N
Assay: Ratio of Alkyl components.n-C12H25 homolog 0 Character N N N
Assay: Ratio of Alkyl components.n-C14H29 homolog 0 Character N N N
Assay: Total alkyl benzyldimethylammonium chlorides. (By: Titrimetry) 0 Character N N N
Assay:(A mixture of Epimers A and B C25H34O6, On dried basis) 0 Character N N N
Assay:. by HPLC Each 5 ml of the reconstituted suspension Cefadroxil IP Equivalent to anhydrous Cefadroxil 250 mg. 0 Character N N N
Average Fill Weight 0 Character N N N
Average filled Volume 0 Character N N N
Average weight 0 Character N N N
Average weight (Only cap) (g) 0 Character N N N
Avg.weight 0 Character N N N
Avibactam content ( By HPLC on as is basis ) 0 Character N N N
Avibactam Sodium Content (By HPLC on as is basis) 0 Character N N N
Azithromycin Impurity (B) 0 Character N N N
Azithromycin IP 250 mg: 0 Character N N N
B) 0 Character N N N
B) Sodium Test 0 Character N N N
B) Assay (After 7th day)by HPLC Each 5 ml reconstituted suspension contains:Cefixime IP (as Trihydrate) equivalent to Anhydrous Cefixime 100 mg. 0 Character N N N
b) 5 ml marking 0 Character N N N
B) Acid value 0 Character N N N
B) Assay (After 7th day) by HPLC 0 Character N N N
B) Assay (After 7th day) Cephalexin IP equivalent to anhydrous Cephalexin 125 mg. 0 Character N N N
B) Assay (After 7th day) Each 5 ml of the reconstituted suspension contains:Cefixime IP as Trihydrate equivalent to anhydrous Cefixime 100 mg. 0 Character N N N
B) Assay (After 7th day): Each 5 ml reconstituted suspension contains: Cefixime Trihydrate IP equivalent to Cefixime anhydrous 40 mg 0 Character N N N
B) Assay (in %) (Each vial contains: Sulbactam Sodium USP eq. to Anhydrous Sulbactam) % 0 Numeric Range N N N
B) Assay (in %) Sulbactam Sodium USP Eq.to Sulbactam (%w/w) 0 Numeric Range N N N
B) Azithromycin 0 Character N N N
B) Azithromycin by HPLC 0 Character N N N
B) By Sodium 0 Character N N N
B) By Acid Value of Fatty Acid 0 Character N N N
B) By Assay Test 0 Character N N N
B) By Chemical 0 Character N N N
B) By Chemical test 1 0 Character N N N
B) By Colour test 0 Character N N N
B) By GC 0 Character N N N
B) By HPLC 0 Character N N N
B) By IR 0 Character N N N
B) By Light obscuration particle count test 0 Character N N N
B) By Light obscuration particle count test 0 Character N N N
B) By Melting point 0 Character N N N
B) By Refractive index 0 Character N N N
B) By TLC 0 Character N N N
B) By UV 0 Character N N N
B) By Viscosity: Degree of polymerization 0 Character N N N
B) Cefoperazone 0 Character N N N N
B) Cefoperazone (activity) 0 Character N N N N
B) Clarity with acetic acid 0 Character N N N
B) Hydroxyl value 0 Character N N N
B) Individual net volume 0 Character N N N
B) Limit of Diethylene glycol and ethylene glycol: 0 Character N N N
B) NLT 70 % (Q) i.e 75 % of the labeled amount of cefuroxime released in 45 min. 0 Character N N N
B) NLT 75% (D) i.e 80 % of the stated amount of Ofloxacin released in 45 min. 0 Character N N N
b) NMT 20.0% particles should retain on #200 mesh ASTM (75µm) 0 Character N N N
B) Ofloxacin released in 45 min. 0 Character N N N
B) Salmonella 0 Character N N N
B) Salmonellae and Shigella 0 Character N N N
B) Sodium salt Test 0 Character N N N
B) Test of sodium 0 Character N N N
B) Total fungal count 0 Character N N N
B) Total molds and yeasts count 0 Character N N N
B)1 For Ofloxacin % Single Maximum Impurity: 0 Character N N N
B)2 For Ofloxacin % Total Impurities: 0 Character N N N
B)Assay (After 7th day of reconstitution) by HPLC Cefixime USP (as Trihydrate) equivalent to Anhydrous Cefixime 50 mg. 0 Character N N N
B)Assay (After 7th day) by HPLC Cefpodoxime Proxetil IP equivalent to Cefpodoxime 50 mg.. 0 Character N N N
B)Assay (After 7th day) by HPLC Each 5 ml reconstituted suspension contains:Cefixime Trihydrate IP equivalent to Cefixime anhydrous 50 mg. 0 Character N N N
B)Assay (After 7th day) by HPLCEach 5 ml reconstituted suspension contains: Cefixime Trihydrate IP equivalent to Cefixime 0 Character N N N
B)Assay (After 7th day) by HPLCEach 5 ml reconstituted suspension contains: Cefixime Trihydrate IP equivalent to Cefixime anhydrous 50 mg. 0 Character N N N
B)Assay (After 7th day) by HPLCEach 5 ml reconstituted suspension contains: Ofloxacin IP 50 mg:. 0 Character N N N
B)By HPLCEach 5 ml of the reconstituted suspension Assay (After 7th day) contains:Cefpodoxime Proxetil IP equivalent to Cefpodoxime 50 mg. 0 Character N N N
b)NLT 75 % (Q) i.e 80 % of the labeled amount of cefuroxime released in 45 min. 0 Character N N N
B)NLT 90% of L.C the stated amount of Ofloxacin released in 45 min. 0 Character N N N
B)Solution A with strong hydrogen peroxide solution produces orange- red colour . 0 Character N N N
B)Specific Microbial Limit (Pathogens) 0 Character N N N
B)Total fungal count 0 Character N N N
B- The sum of stearic acid and palmitic acid 0 Character N N N
B. Total unknown impurities apart from 2-butanol 0 Character N N N
B.Degree of Polymerization 0 Character N N N
B.Thiazolylacetyl glycine oxime acetal 0 Character N N N
B.Total Impurities other than 2-Butanol 0 Character N N N
B1) For Ceftriaxone % Single Maximum unknown impurity: 0 Character N N N
B1) for ≥ 10µ 0 Character N N N
B2) For Ceftriaxone % Total unknown impurity 0 Character N N N
B2) for ≥ 25µ 0 Character N N N
Bacterial Endotoxin 0 Character N Y N
Bacterial Endotoxin (Endotoxin Unit per mg for both ) 0 Character N Y N
Bacterial Endotoxin Test 0 Character N N N
Bacterial Endotoxin test: 0 Character N N N
Barcode 0 Character N N N
Barium 0 Character N N N
Base colour 0 Character N N N
Base Outer Diameter 0 Character N N N
Benzene 0 Character N N N
Benzene and related substances by GC 0 Character N N N
Benzoate 0 Character N N N
Benzoic Acid 0 Character N N N
Bile tolerant gram-negative Bacteria 0 Character N N N
Bled Uniformity. 0 Character N N N N
Bleeding 0 Character N N N
Board Grammage 0 Character N N N
Board quality 0 Character N N N
Body Outer Diameter (mm) 0 Character N N N
Boiling Range 0 Character N N N
Bottom Layer 0 Character N N N
Bottom Outer Dia (mm) 0 Character N N N
Braille Test 0 Character N N N
Bromide 0 Character N N N
Bromide and Iodide 0 Character N N N
Bromide: By Visible absorption spectroscopy 0 Character N N N
Bromoacetyl analog 0 Character N N N
BUDATE BACK LABEL TRANSPULE 0 Character N N N
BUDATE BACK LABLE TRANSPULE 0 Character N N N
BUDATE BACK LABLE TRANSPULE 271771 0 Character N N N
Budate Carrugated Box 525x340x305 mm 0 Character N N N
BUDATE CARTON 0 Character N N N
BUDATE FRONT LABEL 0 Character N N N
BUDATE POUCH LABEL 0 Character N N N
BUDATE TRANSPULE PRINTED INSERT 0 Character N N N
BUDECORT RESPULES 0.5 MG POUCH LABEL 0 Character N N N
Buffering Capacity 0 Character N N N
Buffering capacity 0 Character N N N
Bulk Density 0 Character N N N
Bulk Density 0 Character N N N
Burst factor 0 Character N N N
Burst strength 0 Character N N N
Bursting Strength (kg/cm2) 0 Character N N N
By HPLC 0 Character N N N
By IR 0 Character N N N
C) 0 Character N N N
c) 10 ml marking 0 Character N N N
C) Absorbance at 430nm (10 % w/v solution in water) 0 Character N N N
C) By Chemical 0 Character N N N
C) By Chemical test 0 Character N N N
C) By chemical test 2 0 Character N N N
C) By GC 0 Character N N N
C) By HPLC 0 Character N N N
C) By IR# 0 Character N N N
C) By Sodium test 0 Character N N N
C) By TLC 0 Character N N N
C) By UV 0 Character N N N
C) Escherichia coli 0 Character N N N
C) Pathogen count 0 Character N N N
C) Pseudomonas aeruginosa 0 Character N N N
C) Test of sodium 0 Character N N N
C)Escherichia coli 0 Character N N N
C)Solution A with zinc granules produces a violet blue colour. 0 Character N N N
C. Cefdinir Sulfoxide 0 Character N N N
Cadmium ( as Cd ) 0 Character N N N
Cadmium (as Cd) 0 Character N N N
calcium 0 Character N N N
Calcium and Magnesium 0 Character N N N
Calcium and magnesium ( Calculated as Ca) 0 Character N N N
Calcium and magnesium: 0 Character N N N
Caliper 0 Character N N N
Caliper(thickness) 0 Character N N N
Cap Fitment & Sealing 0 Character N N N
Cap Height 0 Character N N N
Cap ID 0 Character N N N
Cap OD 0 Character N N N
Cap weight 0 Character N N N
Caproic acid: 0 Character N N N N
Caprric acid: 0 Character N N N N
Caprylic acid: 0 Character N N N N
Carbonates 0 Character N N N
Cefadroxil Impurity-A 0 Character N N N
Cefadroxil Impurity-B 0 Character N N N
Cefadroxil IP Equivalent to anhydrous Cefadroxil 250 mg 0 Character N N N
Cefadroxil IP equivalent to Anhydrous Cefadroxil 500 mg 0 Character N N N
Cefadroxil IP equivalent to Anhydrous Cefadroxil125 mg. 0 Character N N N
Cefdinir USP equivalent to anhydrous Cefdinir 300 mg. 0 Character N N N
cefepime 0 Character N N N
Cefepime Hydrochloride IP eq. to Cefepime % 0 Numeric Range N N N
Cefepime Impurity (A) 0 Character N N N
Cefepime Impurity (B) 0 Character N N N
Cefepime Related Compound A 0 Character N N N
Cefepime Related Compound C 0 Character N N N
Cefetamet 0 Character N N N
Cefixime 200 mg:Ofloxacin IP 200 mg: 0 Character N N N
Cefixime Trihydrate IP equivalent to anhydrous 0 Character N N N
Cefixime Trihydrate IP equivalent to anhydrous Cefixime 100 mg.. 0 Character N N N
Cefixime Trihydrate IP equivalent to anhydrous Cefixime 200 mg. 0 Character N N N
Cefixime Trihydrate IP equivalent to Cefixime 0 Character N N N
Cefixime Trihydrate IP equivalent to Cefixime (Anhydrous) 50 mg. 0 Character N N N
Cefixime Trihydrate IP equivalent to Cefixime anhydrous 50 mg. 0 Character N N N
Cefixime Trihydrate USP equivalent to anhydrous Cefixime 200 mg. 0 Character N N N
Cefixime Trihydrate USP equivalent to Cefixime (Anhydrous) 100 mg. 0 Character N N N
Cefixime USP (as Trihydrate) equivalent to Anhydrous Cefixime 100 mg. 0 Character N N N
Cefixime USP (as Trihydrate) equivalent to Anhydrous Cefixime 50 mg 0 Character N N N
Cefoperazone 0 Character N N N N
Cefoperazone Sodium IP Eq. to Cefoperazone 0 Character N N N
Cefoperazone Sodium USP Eq. to Cefoperazone 0 Character N N N
Cefotaxime dimer 0 Character N N N
Cefotaxime open ring lactone 0 Character N N N
Cefotaxime related compound E 0 Character N N N
Cefotaxime sodium (sterile) USPeq. to Cefotaxime 500 mg 0 Character N N N
Cefotaxime Sodium equivalent to Cefotaxime in (%) Labeled Amount 0 Character N N N
Cefpodoxime Proxetil IP equivalent to Cefpodoxime 100 mg. 0 Character N N N
Cefpodoxime Proxetil IP equivalent to Cefpodoxime 100 mg. 0 Character N N N
Cefpodoxime Proxetil IP equivalent to Cefpodoxime 200 mg. 0 Character N N N
Cefpodoxime Proxetil IP equivalent to Cefpodoxime 50 mg.. 0 Character N N N
Ceftazidime pentahydrate equivalent to Ceftazidime (C22H22N6O7S2) In (%) Labeled Amount 0 Character N N N
Ceftriaxone -3-ene isomer 0 Character N N N
Ceftriaxone benzothiazolyoxime 0 Character N N N
Ceftriaxone E-Isomer 0 Character N N N
Ceftriaxone Sodique BP (Sterile) Equivalent to Ceftriaxone 1000 mg 0 Character N N N
Ceftriaxone Sodium IP (Sterile) eq. to Anhydrous Ceftriaxone 0 Character N N N
Ceftriaxone Sodium IP eq. to anhydrous Ceftriaxone 0 Character N N N
Ceftriaxone Sodium IP Eq. to Ceftriaxone 0 Character N N N
Ceftriaxone Sodium USP eq. to Ceftriaxone 0 Character N N N
Ceftriaxone triazine analog 0 Character N N N
Ceftriaxone USP On Anhydrous Basis 0 Character N N N
Cefuroxime 0 Character N N N
Cefuroxime axetil dimer 0 Character N N N
Cefuroxime Axetil D³-isomers 0 Character N N N
Cefuroxime Axetil E-isomers 0 Character N N N
Cefuroxime Axetil equivalent to Cefuroxime (C16H16N4O8S), in mg (%) Labeled amount 0 Character N N N
Cefuroxime Axetil IP equivalent to 0 Character N N N
Cefuroxime Axetil IP equivalent to Cefuroxime 250 mg. 0 Character N N N
Cefuroxime Axetil IP equivalent to Cefuroxime 500 mg. 0 Character N N N
Cefuroxime Axetil USP equivalent to 0 Character N N N
Cefuroxime Axetil USP equivalent to Cefuroxime 125 mg. 0 Character N N N
Cefuroxime Axetil USP equivalent to Cefuroxime 500 mg. 0 Character N N N
Cefuroxime lactone 0 Character N N N
Chloride 0 Character N N N
Chlorides 0 Character N N N
Chlorinated Compounds 0 Character N N N
Chromatographic Purity 0 Character N N N
Chromatographic Purity (%) (By HPLC) 0 Character N N N
Chromatographic purity* (By HPLC) 0 Character N N N
Cinnamic Acid 0 Character N N N
CIPLOX-D EYE/EAR DROP CARTON 10 ML 0 Character N N N
CIPLOX-D EYE/EAR DROPS 10 ML LABELS 0 Character N N N
Claim 0 Character N N N
Clarity of Solution 0 Character N N N
Cleanliness 0 Character N N N
Code no is missing 0 Character N N N
Code No. is missing or is not in accordance with the standard 0 Character N N N
Color (425nm,cmcell) 6.2ml WFI/vial 0 Character N N N N
Color index (10% solution w/v ) 0 Character N N N N
Color of Reconstituted Solution 0 Character N N N
color of solution 0 Character N N N
colorant 0 Character N N N
Colour 0 Character N N N
Colour Absorbance 0 Character N N N
Colour Index Absorbance of a 5% w/v solution of sample at 240nm is not more than 0.060. 0 Character N N N
Colour Index (5g in 50 ml) 0 Character N N N
Colour Lake Sun Yellow 0 Character N N N
Colour lifting 0 Character N N N
Colour Of Flip Off Disc 0 Character N N N
Colour of solution (By UV) 0 Character N N N
Colour scheme 0 Character N N N
Colour Shade 0 Character N N N
colour shade of kraft paper 0 Character N N N
Colour Value 0 Character N N N
Colouring matter 0 Character N N N
Combined Ether Extracts 0 Character N N N
Compound A (Aminosulfinic acid) 0 Character N N N
Compound A (Aminosulfinic acid)Individual Impurity 0 Character N N N
Compressibility index 0 Character N N N
Compression strength 0 Character N N N
Condition of Core 0 Character N N N
Condition of Roll 0 Character N N N
Conductivity 0 Character N N N
Congealing Temperature 0 Character N N N
Constituted solution 0 Character N N N
Constituted solution (Clarity of solution ) 0 Character N N N
Constituted solution (Completeness & Clarity of Solution ) 0 Character N N N
Constituted Solution, Completeness and clarity of solution (1g in 10 ml ) 0 Character N N N
Content of 2,3, cyclopentane 5 pyridine 0 Character N N N
Content of Water soluble material 0 Character N N N
Content of Arginine 0 Character N N N
Content of Avibactam sodium equivalent to Avibactam 0 Character N N N
Content of Cefepime 0 Character N N N
Content of Ceftazidime on as is basis 0 Character N N N
Content of ceftazidime pentahydrate equivalent to ceftazidime 0 Character N N N
Content of Glycopyrrolate equivalent to Glycopyrronium 0 Character N N N N
Core Diameter (mm) 0 Character N N N N
Core used 0 Character N N N
Creasing Quality 0 Character N N N
Crystallinity 0 Character N N N
Cutting and Creasing 0 Character N N N
Cyclohexane 0 Character N N N
D) 0 Character N N N
D) By Chemical 0 Character N N N
D) Chemical test 0 Character N N N
D) Salmonella 0 Character N N N
D) Staphylococcus aureus 0 Character N N N
D) TLC 0 Character N N N
D)By Melting point 0 Character N N N
D)Salmonella spp. 0 Character N N N
D-Phenylglycine 0 Character N N N
D. Cefdinir thiazine analog 0 Character N N N
D10 0 Character N N N
D3- isomers 0 Character N N N
d50 0 Character N N N
d90 0 Character N N N
d97 0 Character N N N
Deacetylcefotaxime lactone 0 Character N N N
Deacyl Ceftriaxone 0 Character N N N
Degree of Polymerization 0 Character N N N
Degree of substitution (on dried basis) 0 Character N N N
Deliverable volume 0 Character N N N
Descarbamoyl – cefuroxime Impurity 0 Character N N N
Descorbomoyl Cefuroxime Impurity 0 Character N N N
Description A clear or almost clear, Oily, yellowish or brownish yellow liquid, Odour faint and Charateristic. 0 Character N N Y
Design 0 Character N N N
Dexamethasone content 0 Character N N N
Dextrins 0 Character N N N
Diameter (in mm) 0 Character N N N
Diameter Of Flip- Off Disc 0 Character N N N
Diameter Of Wad(mm) 0 Character N N N
Diastereoisomer ratio 0 Character N N N
Dichloromethane 0 Character N N N
Didehydroglycopyrrolate 0 Character N N N N
Differential scanning calorimetry 0 Character N N N
Diglyme ether 0 Character N N N N
Dimethyl Formamide 0 Character N N N N
Disintegration Test 0 Character N N N
Dispersion Time 0 Character N N N
Dissolution (% Drug Release) 0 Character N N N
Dissolution By UV 0 Character N N N
Distillation Range 0 Character N N N
Dodecane 0 Character N N N N
Dye Content 0 Character N N N
E coli 0 Character N N N
E) 0 Character N N N
E) By chemical 0 Character N N N
E) Pseudomonas Aeruginosa 0 Character N N N
E)Pseudomonas Aeruginosa 0 Character N N N
E- isomers 0 Character N N N
E-Cefotaxime 0 Character N N N
E. Cefdinir impurity 1 0 Character N N N
E. coli 0 Character N N N
Each 5 ml of the reconstituted suspension contains:Cephalexin IP equivalent toanhydrous Cephalexin 125 mg. 0 Character N N N
Each film coated tablet contains: Cefuroxime Axetil USP equivalent to Cefuroxime 250 mg 0 Character N N N
Each film coated tablet contains:Cefpodoxime Proxetil IP equivalent to Cefpodoxime200 mg. 0 Character N N N
Each Hard gelatin capsule contains: Amoxycillin Trihydrate IP eq. to amoxycillin 0 Character N N N N
Each tablet contains: Cephalexin equivalent to Anhydrous Cephalexin 250 mg. % 0 Numeric Range N N N N
Each tablet contains:Cephalexin equivalent to Anhydrous Cephalexin 125 mg. 0 Character N N N
Each vial contains Cefazolin sodium equivalent to Cefazolin in mg In (%) Labeled Amount 0 Character N N N
Each vial contains Cefuroxime Sodium equivalent to Cefuroxime (C16H16N4O8S), in mg 0 Character N N N
Each vial contains: Ceftriaxone Sodium IP Eq. to Ceftriaxone % 0 Numeric Range N N N
Each vial contains: Ceftriaxone Sodium USP eq. to Ceftriaxone 0 Character N N N
Each vial contains:Cefotaxime Sodium IP eq. to Cefotaxime 0 Character N N N
Each vial contains:Cefotaxime sodium USP eq. to cefotaxime 0 Character N N N
Each vial contains:Cefuroxime Sodium IP eq. to Cefuroxime % 0 Numeric Range N N N
Elasticity Identification 0 Character N N N
Enantiomeric Purity: By HPLC (S)- Salbutamol Sulphate 0 Character N N N N
Enmetazobactam 0 Character N N N
Enterobacteriaceae Should be absent 0 Character N Y N
Epimer A: By HPLC Not Less Than 40.0 and Not More Than51.0 0 Character N N N
Escherichia coli 0 Character N N N
Ethanol 0 Character N N N
Ethanol by GC 0 Character N N N
Ether -Soluble Substances 0 Character N N N
Ether Extractable matter 0 Character N N N
Ethyl Acetate 0 Character N N N
Ethylene dichloride 0 Character N N N N
Ethylene glycol & diethylene glycols( by GC ) 0 Character N N N
Extractable Heavy metals Extractable Heavy metals 0 Character N N N
Extractable Volume 0 Character N N N
Extractable ZINC 0 Character N N N
F) Staphylococcus 0 Character N N N
F)Staphylococcus aureus 0 Character N N N
F. 3-Methyl Cefdinir 0 Character N N N
Face Paper 0 Character N N N
Face stock 0 Character N N N N
Fatty acid composition ( by GC ) 0 Character N N N
Ferrocyanide 0 Character N N N
Fill weight 0 Character N N N N
Fill weight (Average) (20 vials) (Individual) 0 Character N N N N
Fill weight (Average) (20 vial) 0 Character N N N N
Fill weight (Average) (20 vials) (Individual) 0 Character N N N N
First substrate (PET) GSM 0 Character N N N
Fitting 0 Character N N N
Fitting of screw cap with bottle 0 Character N N N
Flange Thickness (Collar) Flange Thickness (Collar) 0 Character N N N
Flavour / odor 0 Character N N N
Flavour Strength 0 Character N N N
Flavour/Odor 0 Character N N N
Fluorences 0 Character N N N
Fluorescent Impurity 0 Character N N N
Fluoroquinolonic acid: (By TLC) 0 Character N N N
Flute 0 Character N N N
Flute 1 0 Character N N N
Flute 3 0 Character N N N
flute2 0 Character N N N
Fluticasone acetate 0 Character N N N N
Fluticasone acid 0 Character N N N N
Fluticasone acid Propionate 0 Character N N N N
Foil thickness (mm) 0 Character N N N
Folding 0 Character N N N
Folding Quality 0 Character N N N
Folding Size (Width mm) 0 Character N N N
Folding Size (Length mm) 0 Character N N N
for ≥ 10µ 0 Character N N N
for ≥ 25µ 0 Character N N N
For , nominal volume of more than 5 ml 0 Character N N N
for > 10 ml volume 0 Character N N N
For Arginine 0 Character N N N
For Avibactam 0 Character N N N
For Cefepime 0 Character N N N
For CEFIXIME 0 Character N N N
For Ceftazidime 0 Character N N N
For Glycopyrronium < By HPLC> 0 Character N N N N
For Ofloxacin 0 Character N N N
for ¡Ü 10 ml volume 0 Character N N N
For, nominal volume of 5 ml or less than 5 ml 0 Character N N N
Foreign Amines 0 Character N N N
Foreign matter 0 Character N N N
Foreign matter(6.2 ml of WFI/vial) 0 Character N N N N
Formic acid 0 Character N N N
Fourth substrate (Poly) GSM 0 Character N N N
Fragmentation Test 0 Character N N N
Free Chlorine 0 Character N N N
Free Dye Content 0 Character N N N
Free fatty acids 0 Character N N N
Free stearic acid 0 Character N N N
Freezing point 0 Character N N N
Friability 0 Character N N N
Fumaric Acid Content: (By HPLC) 0 Character N N N N
fungus(cfu/g) Not more than 100 0 Character N Y N
G. Cefdinir Related compound A 0 Character N N N
Gap between labels 0 Character N N N
Glass Grains Test(ml) 0 Character N N N
Glucose and invert sugar 0 Character N N N
Glycopyrrolate Related Compound B 0 Character N N N
Glycopyrrolate Related Compound C 0 Character N N N
Glycopyrrolate Related compound I 0 Character N N N
Glycopyrrolate Related Compound L 0 Character N N N
Grade 0 Character N N N N
Grain Direction 0 Character N N N
Gramage Of Aluminium Foil Without VMCH/HSL/Universal HSL 0 Character N N N
GramageOf VMCH/HSL/Universal HSL Coating 0 Character N N N
Grammage (gsm) 0 Character N N N
Grammage Of Polythene 0 Character N N N
Grammage Of Aluminium Foil Without Polythene 0 Character N N N
Grammage of Bottom Layer 0 Character N N N
Grammage of each ply 0 Character N N N
Grammage of each ply Layer-2:- NLT 126 GSM 0 Character N N N
Grammage of each ply Layer-3:- NLT 126 GSM 0 Character N N N
Grammage of each ply Layer-4:- NLT 126 GSM 0 Character N N N
Grammage of each ply Layer-5:- NLT 126 GSM 0 Character N N N
Grammage of Layer-2 0 Character N N N
Grammage of Layer-3 0 Character N N N
Grammage of Layer-4 0 Character N N N
Grammage of Layer-5 0 Character N N N
Grammage of Middle Layer 0 Character N N N
Grammage of Top Layer 0 Character N N N
Grammage of Top Ply 0 Character N N N
GSM 0 Character N N N
GSM Adhesive 0 Character N N N
GSM Adhesive Paper 0 Character N N N
GSM Face Paper : 0 Character N N N
GSM Release Paper 0 Character N N N
GSM (gm/sq. meter) 0 Character N N N
GSM of face stock 0 Character N N N
GSM Of Paper (G/m2) 0 Character N N N N
GSM of PVDC Coating 0 Character N N N
Guage of aluminium 0 Character N N N
GUM 0 Character N N N N
H.Cefdinir Related compound A 0 Character N N N
Halogenated compounds 0 Character N N N
Hardness 0 Character N N N
Hausner ratio 0 Character N N N
Heat seal lacquer 0 Character N N N
Heat seal lacquer coating part 0 Character N N N
Heavy metals 0 Character N N N
Height 0 Character N N N
Height (mm) 0 Character N N N
Height of Partition 0 Character N N N
Height of plastic Disc (mm) 0 Character N N N
Height of Seal Aluminium portion (mm) 0 Character N N N
Hexane (ppm) 0 Character N N N
Highest Individual Impurity 0 Character N N N
HSL coating grammage 0 Character N N N
HSL GSM 0 Character N N N
HYDRAZINE 0 Character N N N
Hydrolytic Resistance (ml) 0 Character N N N
Hydroxyl value 0 Character N N N
Hydroxypropoxy 0 Character N N N
Hydroxypropyl Group 0 Character N N N
i) Ethylene Glycol 0 Character N N N N
i) Escherichia coli 0 Character N N N
i) Ethylene Glycol 0 Character N N N
i)Methonol 0 Character N N N
i)Total aerobic microbial count 0 Character N N N
I. Cefdinir Related compound A 0 Character N N N
ID of Mouth 0 Character N N N
Identification A blue colour is produce on treatment of the sample with chloroform, Potassium thiocyanate and Cobal 0 Character N N N
Identification B : By Thin layer chromatography 0 Character N N N
Identification C The sample solution decolourises bromine water. 0 Character N N N
Identification C : By HPLC 0 Character N N N
Identification (By : IR ) 0 Character N N N
Identification (By Ferric Oxide Test) 0 Character N N N
Identification (By HPLC) 0 Character N N N
Identification (By TLC) 0 Character N N N
IDENTIFICATION A 0 Character N N N
Identification A 0 Character N N N
Identification A For Sodium 0 Character N N N N
Identification B 0 Character N N N
Identification B (By HPLC) 0 Character N N N
Identification B For Chloride 0 Character N N N N
Identification B: (By TLC) 0 Character N N N
Identification By GC 0 Character N N N
Identification By uv 0 Character N N N
Identification C 0 Character N N N
Identification D The Infrared absorption spectrum of sample is concordant with the infrared absorption spectrum of Po 0 Character N N N
Identification for aluminium 0 Character N N N
Identification of Nitrocellulose Coating 0 Character N N N
Identification of PE ( sealant layer ) by IR 0 Character N N N
Identification: (By UV) 0 Character N N N
ii) Diethylene Glycol 0 Character N N N N
ii) Diethylene Glycol 0 Character N N N
ii) P.aeruginosa 0 Character N N N
ii)Ethanol 0 Character N N N
ii)Total molds and yeasts count 0 Character N N N
iii) Triethyene Glycol 0 Character N N N N
iii) S.aureus 0 Character N N N
iii) Triethylene Glycol 0 Character N N N
iii)Acetone 0 Character N N N
IMPURITY -A By -HPLC 0 Character N N N
Impurity A 0 Character N N N
Impurity A (BY TLC) 0 Character N N N N
Impurity B 0 Character N N N
Impurity C 0 Character N N N
Impurity D 0 Character N N N
Impurity E 0 Character N N N
Impurity F 0 Character N N N
Impurity G 0 Character N N N N
Impurity H 0 Character N N N N
Impurity I 0 Character N N N N
Inadequate space for batch details 0 Character N N N
Individual (GSM) 0 Character N N N
Individual (GSM)* 0 Character N N N
Individual Impurity 0 Character N N N
Induction Wad Thickness 0 Character N N N
Initia pH: 0 Character N N N
Ink Details 0 Character N N N
Ink Grade 0 Character N N N
Ink lifting test 0 Character N N N
Ink Shade 0 Character N N N
Inner flap Height(mm) 0 Character N N N
Inner core diameter 0 Character N N N
Inner diameter 0 Character N N N
Inner Diameter of Aluminium Seal (mm) 0 Character N N N
Inner Height of Aluminium seal 0 Character N N N
Inorganic Phosphate : By ultraviolet and visible absorption spectrophotometry Calculated as Po4 0 Character N N N
Inside Height (mm) 0 Character N N N
Insoluble in HCl 0 Character N N N
Insoluble substances 0 Character N N N
Internal Dia (mm) 0 Character N N N
Internal Diameter (mm) 0 Character N N N
Internal Mouth Diameter 0 Character N N N
Internal Mouth Diameter(mm) 0 Character N N N
Iodide 0 Character N N N
Iodides 0 Character N N N N
Iodine value 0 Character N N N
Iron 0 Character N N N
Iron Test 0 Character N N N
Iso-propanol 0 Character N N N
Isomer Ratio (By HPLC) 0 Character N N N
Isopropyl Alcohol 0 Character N N N
iv) Salmonella 0 Character N N N
iv)Isopropyl Alcohol 0 Character N N N
J. Cefdinir Related compound A 0 Character N N N
K-value 0 Character N N N
K. 7-s Cefdinir 0 Character N N N
L. Cefdinir Lactone 0 Character N N N
Label grade 0 Character N N N N
Label manufacturer 0 Character N N N N
LABEL TAMPER EVIDENT FOR MID-MIDAS 0 Character N N N
Labels with missing print 0 Character N N N
Lactic Acid Bacillus 60 million Spores 0 Character N N N
Lactic acid producing capacity 0 Character N N N
Laminated ALU Foil 0 Character N N N
Lauric acid: 0 Character N N N N
LDPE film Grammage 0 Character N N N
Lead 0 Character N N N
Lead (as Pb ) 0 Character N N N
Lead (as Pb) 0 Character N N N
Lead and Heavy Metals 0 Character N N N
Leak Test 0 Character N N N
Length 0 Character N N N
Length (mm) 0 Character N N N
Length After Folding 0 Character N N N
Length of Partition 0 Character N N N
Less than 10 ml volume 0 Character N N N
Levosalbutamol Assay Duolin 0 Character N N N N
Light Absorption 0 Character N N N
Light absorption (Solution A) 0 Character N N N
Light Absorption (by UV) at 440 nm 0 Character N N N
Light absorption : by ultraviolet and visible absorption spectrophotometry 0 Character N N N
Limit (In % w/w) 0 Character N N N
Limit of , Benzaldehyde 0 Character N N N
Limit of Aluminum %w/w 0 Character N N N
Limit of amines and amine salts (By: potentiometry) 0 Character N N N
Limit of Benzyl Alcohol (By: HPLC) 0 Character N N N
Limit of bromides 0 Character N N N N
Limit of Cadmium (ppm) 0 Character N N N
Limit of Calcium %w/w 0 Character N N N
Limit of Chloromethyl benzene : 0 Character N N N
Limit of Erythro Isomer; (By HPLC) 0 Character N N N
Limit of Hydrogen chloride 0 Character N N N
Limit of Iron %w/w * 0 Character N N N
Limit of Lead ppm 0 Character N N N
Limit of Methacrylic Acid and Ethyl Acrylate 0 Character N N N
Limit of N – Methyl pyrrolidine (%w/w) 0 Character N N N
Limit of Nickel (ppm) 0 Character N N N
Limit of nitrilotriacetic acid 0 Character N N N N
Limit of Nonvolatile Residue 0 Character N N N
Limit of oxalic acid 0 Character N N N N
Limit of phosphates 0 Character N N N N
Limit of Pyridine % (w/w) * 0 Character N N N
Liner GSM 0 Character N N N
Liner GSM 0 Character N N N
Linoleic acid 0 Character N N N N
Linoleic acid: 0 Character N N N N
Linolenic acid 0 Character N N N N
Lip Thickness (mm) 0 Character N N N
Lock Property 0 Character N N N
Locking 0 Character N N N
Locking Quality 0 Character N N N
LOD ( for 1 hr at 105 ° C ) 0 Character N N N
LOD(%w/w) %w/w 0 Character N N N
Loss on Attrition 0 Character N N N
Loss on drying at 110ºC 0 Character N N N
Loss on Drying (% w/w) (Use 1.0 g sample dry at 105ºC for 3 hours.) 0 Character N N N
Loss on Drying (% w/w) (Use 1g sample dry at 100¢ªC to 105¨¬C for 3 hours.). 0 Character N N N
Loss on Drying (% w/w)(Use 1g sample dry at 100¢ªC to 105¨¬C for 3 hours.). 0 Character N N N
Loss on Drying (%w/w) 0 Character N N N
Loss On Ignition 0 Character N N N
M. Cefdinir Related compound B 0 Character N N N
Magnesium 0 Character N N N
Magnesium and alkaline-earth metals 0 Character N N N N
Manufacturing Joints 0 Character N N N
Marking of 2.5ml,5ml&10ml 0 Character N N N
Material 0 Character N N N
Material Of Flip off Disc 0 Character N N N
MBT Content ( By HPLC, ppm) 0 Character N N N
medium micro 0 Character N N N
Melt flow index 0 Character N N N
Melting Point 0 Character N N N
Melting range 0 Character N N N
Mercury 0 Character N N N
Mercury ( as Hg ) 0 Character N N N
Mercury (as Hg) 0 Character N N N
Methanol 0 Character N N N
Method-IITriethylamine Content 0 Character N N N
Methoxy 0 Character N N N
Methoxyiminofuranyl acetic acid 0 Character N N N
Methyl Bromide Content: (By GC) 0 Character N N N
Methyl Isobutyl Ketone 0 Character N N N
Methylene Chloride 0 Character N N N
Methylene Dichloride 0 Character N N N
Micro Text embossing 0 Character N N N
Microbial Contamination 0 Character N N N
Microbial Enumeration test 0 Character N N N
Microbial Enumeration test (bioburden) 0 Character N N N
Microbial enumeration tests 0 Character N N N
Microbial test 0 Character N N N
Microbial test A)Total viable count ( 1) Total Aerobic Microbial count 0 Character N N N
Microbial test A)Total viable count ( 2)Total Combined Yeast and Mould count 0 Character N N N
Microbial test B) Test for specified microorganism(2) E.coli 0 Character N N N
Microbial test B)Test for specified microorganism (1) Bile tolerant gram- negative bacteria 0 Character N N N
Microbial test B)Test for specified microorganism (3) Salmonella 0 Character N N N
Microbial test B)Test for specified microorganism(4)Pseudomonas aeruginosa 0 Character N N N
Microbial test B)Test for specified microorganism(5)Staphylococcus aureus 0 Character N N N
Microbial test B)Test for specified microorganism(6)Candida albicans 0 Character N N N
Microbial Tests 0 Character N N N
Microbiological examination of non-sterile products: Aerobic Microbial count: 0 Character N N N
Microbiological examination of non-sterile products: Combined Yeasts and Molds count: 0 Character N N N
Microbiological examination of non-sterile products: Total aerobic microbial count. 0 Character N N N
Microbiological examination of non-sterile products: Total combined Yeast and Molds count. 0 Character N N N
Middle Layer 0 Character N N N
Middle Layer-1 0 Character N N N
Middle Layer-2 0 Character N N N
Middle Layer-3 0 Character N N N
Middle layer-4 0 Character N N N
Middle Layer-5 0 Character N N N
Mineral acid 0 Character N N N
Mix up of other product 0 Character N N N
Mix up of other product Cartons 0 Character N N N
Mix up of other product Labels 0 Character N N N
Moisture % 0 Character N N N
Molar Substitution 0 Character N N N
Monocalcium & Tricalcium Phosphates 0 Character N N N
Monosodium phosphate 0 Character N N N
Morphline Test 0 Character N N N
Mouth Inner Diameter (mm) 0 Character N N N
Mouth Outer Diameter (mm) 0 Character N N N
Myristic acid: 0 Character N N N N
N,N-Dimethylacetanide 0 Character N N N
N,N-Dimethylaniline (ppm) 0 Character N N N
n-Butyl acetate 0 Character N N N
n-Decane 0 Character N N N N
N-Hexane 0 Character N N N N
N.Cefdinir isoxazole analog 0 Character N N N
Name of board 0 Character N N N N
Neck Diameter over collar(mm) 0 Character N N N
Neck Diameter over thread(mm) 0 Character N N N
Neck Height (mm) 0 Character N N N
Neck Inner Diameter (mm) 0 Character N N N
Neck Outer Diameter (mm) 0 Character N N N
Neck Ring OD 0 Character N N N
Neck thread OD 0 Character N N N
Neotame Impurity A 0 Character N N N
Net Content 0 Character N N N N
Nickel 0 Character N N N
Nitrate 0 Character N N N
Nitrites 0 Character N N N N
Nitrogen (Method C) 0 Character N N N
Nitrogen (Method II ) 0 Character N N N
Nitrogen (on anhydrous basis) 0 Character N N N
NLT 75% (D) i.e 80 % of the stated amount of Azithromycin released in 45 min. 0 Character N N N
NLT 90% of the stated amount of Cefixime released in 45 min. 0 Character N N N
No of colour 0 Character N N N
No of contener 0 Character N N N
No. of Net 0 Character N N N
No. of corrugated plates 0 Character N N N
No. of cut lock 0 Character N N N
No. of Piles 0 Character N N N
No. of ply (No’s) 0 Character N N N
No. of Slots 0 Character N N N
No. of Track 0 Character N N N
Non volatile Matter 0 Character N N N
Non volatile residue 0 Character N N N
Non-esterified alcohols 0 Character N N N
Not less than 50% (Q) of label claim shall dissolve in 15 min. 0 Character N N N
Not less than 60% (Q) of label claim shall dissolve in 15 min. 0 Character N N N
Not less than 70% (Q) of label claim shall dissolve in 45 min. 0 Character N N N
Not less than 70% (Q) of label claim shall dissolve in 45 min.. 0 Character N N N
Number Of Bridges 0 Character N N N
Number of joints in a roll 0 Character N N N
Number of Joints per Roll 0 Character N N N
o-toluene sulphonamide 0 Character N N N
O. Cefdinir impurity 2 0 Character N N N
OBERVATION 0 Character N N N
OD of Mouth 0 Character N N N
Odour 0 Character N N N
OFLOX-D EYE/EAR DROPS 10 ML LABELS 0 Character N N N
Ofloxacin IP 200 mg 0 Character N N N
Ofloxacin IP 50 mg: 0 Character N N N
Oil Content 0 Character N N N
Oleic acid: 0 Character N N N N
Opening Test 0 Character N N N
optical rotation 0 Character N N N
Organic Colors & Lakes 0 Character N N N
Organic Compounds 0 Character N N N
Organic Impurities 0 Character N N N
Organic Impurities Limit of N–Methyl pyrrolidine (%w/w) 0 Character N N N
Osmolality 0 Character N N N
other polysaccharides 0 Character N N N
Other related substances Total Impurities (excluding 5- Benzyl-3,6-dioxo-2-piperazineacetic acid) 0 Character N N N
Outer flap Height(mm) 0 Character N N N
Outer Dia (mm) 0 Character N N N
Outer Dia Bottom (mm) 0 Character N N N
Outer Diameter (mm) 0 Character N N N
Outer diameter at base 0 Character N N N
Outer Diameter of Aluminium seal (mm) 0 Character N N N
Outer Diameter of flip off seal (mm) 0 Character N N N
Outer Diameter Plastic Portion (mm) 0 Character N N N
Outer Roll Diameter 0 Character N N N
Over flow Capacity (ml) 0 Character N N N
Overall Height 8.00 mm to 8.80 mm 0 Character N N N
Oxalate 0 Character N N N
Oxalic acid 0 Character N N N
Oxidation of Roll 0 Character N N N
Oxidising Substances 0 Character N N N
Oxidizable substances 0 Character N N N
p- toluene sulphonamide 0 Character N N N
p-Hydroxybenzoic acid 0 Character N N N
P. Cefdinir glyoxalic analog 0 Character N N N
P.aeruginosa 0 Character N N N
Packing 0 Character N N N
Palmitic acid 0 Character N N N
Palmitic acid: 0 Character N N N N
Palmitoleic acid 0 Character N N N N
PANTONE 0 Character N N N
Paper 0 Character N N N
Paper Grammage 0 Character N N N
Paper Gsm 0 Character N N N N
Paper Substrate Grade 0 Character N N N
Paper with Adhesive 0 Character N N N
Partical size : X10 Not more than1.0 0 Character N N N
Partical size:X50 Not more than3.0 0 Character N N N
Partical size:X90 Not more than5.0 0 Character N N N
Partical size:X97 Not more than10.0 0 Character N N N
Particle below 20# Sieve 0 Character N N N
Particle below 60# Sieve 0 Character N N N
Particle Size 0 Character N N N
Particle size (By Malvern)-D10 0 Character N N N N
Particle size (By Malvern)-D50 0 Character N N N N
Particle size (By Malvern)-D90 0 Character N N N N
Particle Size (by sieve) 0 Character N N N
Particle Size - D97 0 Character N N N N
Particle Size : X95 0 Character N N N N
Particle Size Distribution (Estimation by analytical sieving) 0 Character N N N
Particle Size-D90 0 Character N N N N
Particle size: 0 Character N N N
Particle size: By Diffraction ( D10 ) 0 Character N N N
Particle size: By Diffraction (D50) 0 Character N N N
Particle size: By Diffraction (D90) 0 Character N N N
Particle size: By Diffraction (D97) 0 Character N N N
Particles ≥ 10µm 0 Character N N N N
Particles ≥ 25µm 0 Character N N N N
Particles≥10pm 0 Character N N N
Particles≥25pm 0 Character N N N
Particulate contamination Equal to greater than 10µm 0 Character N N N N
Particulate contamination Equal to or greater than 25 µm 0 Character N N N N
Particulate Matter NMT 6000 0 Character N N N
Particulate Matter (per gm) 0 Character N N N
Pasting / pre folding 0 Character N N N N
Pasting Quality 0 Character N N N
Pathogens 0 Character N N N
Peel Test 0 Character N N N
Penetrability 0 Character N N N
Performance test 0 Character N N N
Peroxide value 0 Character N N N
Peroxides 0 Character N N N
pH 0 Character N N N
pH ( 10% w/w ) 0 Character N N N
pH ( 2.0 g in 10 ml ) 0 Character N N N
pH (1.0g in 10ml) 0 Character N N N
pH (100 mg of Cefepime per ml) 0 Character N N N
pH (100 mg/ml ) 0 Character N N N
pH (125 g Sulbactam/ml and 250mg cefoperazone/ml) 0 Character N N N N
pH (5 % w/v aqueous solution.) 0 Character N N N
pH (5.0 % w/v suspension in carbon dioxide free water ) 0 Character N N N
pH (Determine in solution A) 0 Character N N N
pH * 0 Character N N N
PH AFTER 7 DAYS 0 Character N N N
pH of 2% Slurry 0 Character N N N
Pharma code No. 0 Character N N N
Pharmacode value 0 Character N N N
Physical Test White and Black Spot should be absent. Top layer of aluminium should not leech/scratch while rubbing 0 Character N N N
Piercing 0 Character N N N
Pin hole count (Nos) * 0 Character N N N
Pin hole count (Nos)* 0 Character N N N
Pin Holes 0 Character N N N
PLAIN CARTON 0 Character N N N
Plug Diameter Plug Diameter 0 Character N N N
Plunger top Diameter 0 Character N N N
Poly foil gsm 0 Character N N N
Poly Gsm 0 Character N N N
Polyamide 0 Character N N N
Polymorphic Identity : By X-Ray Powder Diffraction 0 Character N N N
Potassium 0 Character N N N
Potassium :By flame photometry and atomic absorption spectrophotometry 0 Character N N N
Povidone (PVPK-30) IP 0 Character N N N
Powder fineness(By sieve) 0 Character N N N
Presence of Dirt and Stain 0 Character N N N
Preservative Content 0 Character N N N
Print quality 0 Character N N N
Print repeat length 0 Character N N N
Printability 0 Character N N N
PRINTED POUCH & LAMINATED (LUPIN ) 0 Character N N N
PRINTED POUCH ST LABEL 65 X48 MM 0 Character N N N
Printed text matter 0 Character N N N
Printing 0 Character N N N
Printing Color 0 Character N N N
Printing Matter 0 Character N N N
Printing Quality 0 Character N N N
Printing Surface 0 Character N N N
Propanol 0 Character N N N
Protein 0 Character N N N
Proteinous Impurities 0 Character N N N
pseudomonas aeruginosa 0 Character N N N
Purity: By HPLC 0 Character N N N
PVC 0 Character N N N
PVC BY Morpholine 0 Character N N N
PVC Flim 0 Character N N N
PVC with Adhesive 0 Character N N N
PyrBulk Density 0 Character N N N
Pyridine Content (By HPLC) 0 Character N N N
Pyruvic Acid 0 Character N N N
Q. E-Cefdinir 0 Character N N N
R. Cefdinir decarboxy open ring Lactone a 0 Character N N N
Ratio of Alkyl components. (By: HPLC.) n-C12H25 homolog 0 Character N N N
Reactions of bromides-(A): 0 Character N N N N
Reactions of bromides-(B): 0 Character N N N N
Readily cabonisable substances 0 Character N N N
Readily Oxidisable Substances 0 Character N N N
Reconstitution Time Seconds 0 Character N N N
Reconstitution Time (Seconds) 0 Character N N N
Redispersibility 0 Character N N N
Reducing Impurities 0 Character N N N
Reducing Impurity Not more than 5.0 ml of 0.01 M ceric ammonium sulphate is required. 0 Character N N N
Reducing substances 0 Character N N N
Reducing sugars 0 Character N N N
Reflect Embossing 0 Character N N N
Refractive index 0 Character N N N
Refractive Index @20 ºC º 0 Numeric Range N N N
Related Compound -A 0 Character N N N
Related Compound -B 0 Character N N N
Related Density 0 Character N N N
Related Substance By HPLC (%) 0 Character N N N
Related substances (By UPLC) 0 Character N N N N
Related Substances : (By Thin Layer Chromatography) 0 Character N N N
Related Substances: (By HPLC) i) Ciprofloxacin ethylene diamine analog 0 Character N N N
Related Substances: (By HPLC) ii) Any other Individual impurity 0 Character N N N
Related Substances: (By HPLC)iii) Sum of all Impurities 0 Character N N N
Related Substances: Any secondary peak 0 Character N N N
Related Substances: By HPLC (For Budesonide) 11-Keto Budesonide Impurity 0 Character N N N N
Related Substances: By HPLC (For Budesonide) 21-dehydro budesonide Impurity 0 Character N N N N
Related Substances: By HPLC (For Budesonide) Single maximum unknown Impurity 0 Character N N N N
Related Substances: By HPLC (For Budesonide) Total Impurities 0 Character N N N N
Related Substances: By HPLC (For Formoterol) Formoterol Amine Impurity 0 Character N N N N
Related Substances: By HPLC (For Formoterol) Single Maximum Unknown Impurity 0 Character N N N N
Related Substances: By HPLC (For Formoterol) Total Impurity 0 Character N N N N
Related Substances: By HPLC (Any individual impurity) 0 Character N N N
Related Substances: By HPLC (Total impurity) 0 Character N N N
Related Substances: By HPLC Single maximum impurity 0 Character N N N
Related Substances: Sum of all secondary peaks 0 Character N N N
Relative content of Stearic acid and Palmitic acid (GC Analysis) 0 Character N N N
Relative Density 0 Character N N N
Relative Index 0 Character N N N
Release Paper 0 Character N N N
repeat length 0 Character N N N
Residual Solvent 0 Character N N N
Residual Solvent (by GC) Ethanol 0 Character N N N N
Residual Solvent (By GC) Isopropyl Alcohol Methonol 0 Character N N N N
Residual solvent (Ethyl acetate) 0 Character N N N
Residual solvent by GC (Acetone) Not More Than 5000 0 Character N N N
Residual solvent By GC (Methylene dichloride) Not More Than 600 0 Character N N N
Residual solvent by GC(Acetonitrile) Not More Than 410 0 Character N N N
Residual solvent by GC(Butyraldehyde) Not More Than 100 0 Character N N N
Residual Solvent By GC(Ethyl Acetate) Not More Than 5000 0 Character N N N
Residual solvent By GC(Methanol) Not More Than 1000 0 Character N N N
Residual Solvent Methylene Chloride 0 Character N N N
Residual solvent: (By GC) 2) n-Butanol 0 Character N N N
Residual solvent: (By GC) Methanol 0 Character N N N
Residual solvent: (By GC) Toluene 0 Character N N N
Residual solvent: Acetone 0 Character N N N
Residual solvent: Acetonitrile 0 Character N N N
Residual solvent: Butyraldehyde 0 Character N N N
Residual solvent: Methanol 0 Character N N N
Residual solvent: Methylene dichloride 0 Character N N N
Residual solvent: By :GC Di isopropyl ether 0 Character N N N
Residual Solvent: BY GC Tetrahydrofuran 0 Character N N N
Residual Solvents (By GC) Diethyl ether 0 Character N N N N
Residual Solvents (By GC) Methyl ethyl ketone 0 Character N N N N
Residual solvents (ppm) i)1,4 Dioxane 0 Character N N N
Residual solvents : Name of manufacturer : FEF chemicals 0 Character N N N
Residual solvents :Name of manufacturer: canton laboratories Pvt.Ltd., 0 Character N N N
Residue on evaporation 0 Character N N N
Residue on Ignition 0 Character N N N
Resin 0 Character N N N
Retained on 40# Mesh 0 Character N N N
Retained on 80# Mesh 0 Character N N N
Revision History 0 Character N N N
Rim Thickness 0 Character N N N
Rivision History 0 Character N N N
Roll outer diameter 0 Character N N N N
Rub Resistence 0 Character N N N
S-Methyl Fluticasone 0 Character N N N N
S. Cefdinir decarboxy open ring Lactone b 0 Character N N N
Salmonell sp. 0 Character N N N
Salmonella 0 Character N N N
Saponification value 0 Character N N N
Scuff Proof 0 Character N N N
Scuff Test 0 Character N N N
Sealing Quality 0 Character N N N
Second substrate (PE) GSM 0 Character N N N
Security measures 0 Character N N N
Self Sealing Test 0 Character N N N
Self-Sealiability 0 Character N N N
Settling volume 0 Character N N N
Shade 0 Character N N N
Shigella 0 Character N N N
Shore a Hardness 0 Character N N N
Sieve Analysis 0 Character N N N
Sieve analysis (#% Fines through 60#) % 0 Numeric Range N N N N
Sieve Analysis (#40) 0 Character N N N
Sieve analysis by 30 mesh 0 Character N N N
Single Maximum Impurity 0 Character N N N N
Single Maximum unknown impurity (%): 0 Character N N N
Size of Box 0 Character N N N N
Slot Size 0 Character N N N
Sodium 0 Character N N N
SODIUM BISULPHITE 0 Character N N N
SODIUM BISULPHITE -IP 0 Character N N N
Sodium carbonate (%w/w) * 0 Character N N N
Sodium carbonate content (By Titration) 0 Character N N N
Sodium chloride 0 Character N N N
Sodium chloride & sodium sulphate 0 Character N N N
Sodium chloride and sodium Glycollate (on dried basis) 0 Character N N N
Sodium Chloride IP 0 Character N N N
Sodium Glycollate 0 Character N N N
Solubility 0 Character N N Y
Solubility ammonical solution of copper tetrammine 0 Character N N N
Soluble Chloride & Sulphate (As sodium Salt) 0 Character N N N
Solution S 0 Character N N N
Special Instruction 0 Character N N N
Specific Absorbance 0 Character N N N
Specific Gravity g/ml 0 Character N N N
Specific Optical Rotation (°) 0 Character N N N
Specific Optical Rotation (o) (Calculate on Anhydrous basis) 0 Character N N N
Specific optical rotation: calculated on dried basis. 0 Character N N N
Specific rotation 0 Character N N N
Spoon Cup Height (mm) 0 Character N N N
Spoon Handle Width (mm) 0 Character N N N
Spoon Total Length (mm) 0 Character N N N
Stability of Suspension (After 4 days) 0 Character N N N
Standard Packing 0 Character N N N
Staphylococcus aureus 0 Character N N N
Starch 0 Character N N N
Starch & dextrins 0 Character N N N
Stearic acid 0 Character N N N
Stearic acid and Palmitic acid 0 Character N N N
Stearic acid: 0 Character N N N N
Sterile Ceftriaxone Sodium IP Eq. to Ceftriaxone % 0 Numeric Range N N N
Sterile Tazobactam Sodium Eq.to Tazobactam % 0 Numeric Range N N N
Sterility 0 Character N Y N
Sterility Test 0 Character N N N
Sterility(Membrane filtration method) 0 Character N Y N
Sterilization test 0 Character N N N
Sticking 0 Character N N N
Storage Condition 0 Character N N N
Sulbactam 0 Character N N N N
Sulbactam Related Compound A 0 Character N N N
Sulbactam Related Compound B 0 Character N N N
Sulbactam Related Compound C 0 Character N N N
Sulbactam Related Compound D 0 Character N N N
Sulbactam Related Compound E 0 Character N N N
Sulbactam Related Compound F 0 Character N N N
Sulbactam Sodium BP Eq. to au Sulbactam. 0 Character N N N
Sulbactam Sodium IP Eq. to Sulbactam 0 Character N N N
Sulbactam Sodium IP Eq.to Sulbactam 0 Character N N N
Sulbactam Sodium USP Eq.to Anhydrous Sulbactam % 0 Numeric Range Y N N
Sulbactam Sodium USP Eq.to Sulbactam 0 Character N N N
Sulfate 0 Character N N N
Sulfites 0 Character N N N
Sulfur dioxide 0 Character N N N
Sulphate content 0 Character N N N
Sulphated Ash 0 Character N N N
Sulphated Ash (% w/w) 0 Character N N N
Sulphated Ash (on dried basis) 0 Character N N N
Sulphates 0 Character N N N
Sulphite 0 Character N N N
Sulphites 0 Character N N N
Sum of all secondary impurity 0 Character N N N
Sum of impurities B and C 0 Character N N N
Sum of Impurities other than A and B 0 Character N N N
Sum of impurities other than A and C 0 Character N N N
Supply: 0 Character N N N
Surface finish 0 Character N N N
Surface Glass Test(ml) 0 Character N N N
T-1551B 0 Character N N N N
T-1551E 0 Character N N N N
T-1551F 0 Character N N N N
T. Cefdinir impurity 3 0 Character N N N
Tagger Diameter 0 Character N N N
Tagger Thickness 0 Character N N N
TAMC (Total aerobic microbial count) 0 Character N N N
Tap density 0 Character N N N N
Taped Bulk Density 0 Character N N N
Tapped density 0 Character N N N
Tartrates 0 Character N N N
Taste 0 Character N N N
Tazobactam on anhydrous basis 0 Character N N N
Tazobactam Sodium eq. to Tazobactam 0 Character N N N
Tazobactam Sodium Eq.to Tazobactam % 0 Numeric Range N N N
Tazobactam Sodium on anhydrous basis 0 Character N N N
Technical Defects 0 Character N N N
Test 0 Character N N N
testA 0 Character N N N N
Tetradecane 0 Character N N N N
Tetrahydrofuran 0 Character N N N
Text Matter 0 Character N N N
Text Matter& colour 0 Character N N N
The average volume of suspension should not be less than 100% of the volume declared in the labeling. (NLT 30 ml) 0 Character N N N
Thiazolylglyoxalic methyloxime 0 Character N N N
Thickness 0 Character N N N
Thickness (mm) 0 Character N N N
Thickness of alu. foil 0 Character N N N
Thickness of Aluminium (mm) 0 Character N N N
Thickness of Aluminium Wall (mm) 0 Character N N N
Thickness of BOPP 0 Character N N N
Thickness of metalized polyester film 0 Character N N N
Thickness of polyester film 0 Character N N N
Thickness of polythene 0 Character N N N
Thickness Of Wad(mm) 0 Character N N N
Thickness off sheet (mm) 0 Character N N N
Third substrate (Al foil) GSM 0 Character N N N
Thread Dia (mm) 0 Character N N N
Titanium 0 Character N N N
Toluene 0 Character N N N
Top Diameter 0 Character N N N
Top Layer 0 Character N N N
Top Outer Diameter 0 Character N N N
Total Aerobic Microbial Count NMT 103 cfu/ml 0 Character N N N
Total Aerobic Microbial Count (TAMC) 0 Character N N N
Total Aerobic Microbial Count NMT 1000 cfu/ml 0 Character N N N
Total aerobic microbial count . Not more than 1000 cfu per g 0 Character N N N
Total Ash (%) 0 Character N N N
Total bacterial count 0 Character N N N
Total combined molds and Yeasts count 0 Character N N N
Total combined yeast and molds count 0 Character N N N
Total combined Yeasts and Molds Count NMT 102 cfu/ml 0 Character N N N
Total combined yeasts and molds count . Not more than 100 cfu per g 0 Character N N N
Total combined Yeasts and Molds Count NMT 100 cfu/ml 0 Character N N N
Total degradation product 0 Character N N N
Total degradation product. 0 Character N N N
Total degradation products(excluding Glycopyrrolate related compound C) 0 Character N N N N
Total Dye Content 0 Character N N N
Total Ethanol and Water: The sum of the percentage of Ethanol and the percentage water 0 Character N N N
Total fungi and yeast count 0 Character N N N
Total fungi count 0 Character N N N
Total Gramage Of Aluminium Foil with VMCH/HSL/Universal HSL 0 Character N N N
Total Grammage 0 Character N N N
Total Grammage of Laminate (g/m2) 0 Character N N N N
Total Grammage Of Aluminum Foil 0 Character N N N
Total GSM 0 Character N N N
Total Height 0 Character N N N
Total Height (mm) 0 Character N N N
Total Hight 0 Character N N N
Total Impurities 0 Character N N N
Total Impurities (excluding 0 Character N N N
Total Impurities (excluding Compound A (Aminosulfinic acid) 0 Character N N N
Total impurities other than Ethanol and 2-methylbut -2-ene 0 Character N N N
Total Impurity 0 Character N N N
Total Organic Carbon NMT 8000 ppb. 0 Character N N N
Total secondary Impurities 0 Character N N N
Total Thickness 0 Character N N N
Total unknown impurity (%) 0 Character N N N
Total viable microbial count 0 Character N N N N
Total Weight (mg) 0 Character N N N
Total Weight (gm) 0 Character N N N
Total Yeast and Mold Count (TYMC) 0 Character N N N
Total Yeasts and Molds Count Tests for Specified Micro-Organisms: 0 Character N N N
Transmittance 0 Character N N N
Triethyamine 0 Character N N N
Triethylamine 0 Character N N N
Truxone 1.0 g Sticker label 0 Character N N N
Type 0 Character N N N
Type Of Carton 0 Character N N N
Type of Container 0 Character N N N
Type of flute 0 Character N N N
Type of Varnish 0 Character N N N
Undecane 0 Character N N N N
Uniformity of content 0 Character N N N N
Uniformity of Dispersion 0 Character N N N
Uniformity of dosage units (By weight variation) 0 Character N N N
Uniformity of dosage units By Content Uniformity 0 Character N N N
Uniformity of net filled weight 0 Character N N N
Uniformity of Volume 0 Character N N N
Uniformity of weight 0 Character N N N
Uniformity of weight Fill weight (Average) (20 vial) 0 Character N N N N
Unsaponifiable Matter (%w/w) 0 Character N N N
Unspecified Impurities 0 Character N N N
Unsulfonated primary aromatic amine (Calculated as Aniline) 0 Character N N N
Untaped Bulk Density 0 Character N N N
Unwinding direction 0 Character N N N
User Test 0 Character N N N
v)Dichloro methane 0 Character N N N
Validation 0 Character N N N
Varnish 0 Character N N N
Varnish Details 0 Character N N N
Varnish Grade 0 Character N N N
vi)Ethyl Acetate 0 Character N N N
vii)Methyl isobutyl ketone 0 Character N N N
viii)N-Butyl acetate 0 Character N N N
Vinylpyrrolidinone. 0 Character N N N
Viscosity 0 Character N N N
Viscosity by Rotational Methods mPa.s 0 Character N N N
Visible 0 Character N N N
Visual defects* 0 Character N N N
Visual Foreign Matter 0 Character N N N
Visual Inspection 0 Character N N N
Visual Inspection* 0 Character N N N
Visual Test 0 Character N N N
VMCH Coating 0 Character N N N
VMCH GSM 0 Character N N N
Volatile matter 0 Character N N N
Volatile Oil Content 0 Character N N N
Volatile Sulphides 0 Character N N N
Volume check 0 Character N N N
Volume in Container 0 Character N N N N
wad density 0 Character N N N
Wall Thickness 0 Character N N N
Water Not more than 3.00% w/w 0 Character N N N
Water (% W/W) 0 Character N N N
Water (% w/w) (Use 0.5 g of sample) 0 Character N N N
Water (% W/W) (Use 1.0 g of Sample) 0 Character N N N
Water (%w/w) (Use 0.4 g of sample). 0 Character N N N
Water (%w/w). (Use 0.3g of sample)* 0 Character N N N
Water (%w/w).(Use 0.15gm of sample) 0 Character N N N
Water (KF) 0 Character N N N N
Water (Method I) 0 Character N N N
Water by KF ( % w/w) 0 Character N N N
Water by KF ( % w/w) (Use 0.2g sample). 0 Character N N N
Water by KF (%w/w) (Use 0.1g sample) 0 Character N N N
Water Content 0 Character N N N
Water Content (%w/w) (Determined on 0.5 g) 0 Character N N N
Water determination 0 Character N N N
Water insoluble matter 0 Character N N N
Water soluble substances 0 Character N N N
Water-insoluble matter 0 Character N N N
Water-soluble substances 0 Character N N N
Water: By Karl Fischer 0 Character N N N
Weight 0 Character N N N
Weight (g) 0 Character N N N
Weight of without wad (g) 0 Character N N N
Weight Of 10Flip Off Seal (gm) 0 Character N N N
Weight Of Wad (GM) 0 Character N N N
Weight per ml 0 Character N N N
Weight per ml@20ºC 0 Numeric Range N N N
Weight-Of Tagger (Wad) 0 Character N N N
Width 0 Character N N N
Width (mm) 0 Character N N N
Width After Folding 0 Character N N N N
Width of folding 0 Character N N N
Width of Partition 0 Character N N N
Winding 0 Character N N N
Winding direction 0 Character N N N
winding of Roll 0 Character N N N
Yeast & Mold/G 0 Character N N N
Yeast and Mould Count 0 Character N N N
Zinc stearate 0 Character N N N
ZPL Validation Test Validation Test 0 Character N N N