Valsartan (Page 8 of 8)

VALSARTAN TABLET, FILM COATED

Label Image
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VALSARTAN
valsartan tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50436-2168(NDC:0591-2168)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VALSARTAN (VALSARTAN) VALSARTAN 80 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE
CROSPOVIDONE, UNSPECIFIED
SODIUM LAURYL SULFATE
POVIDONE K30
MAGNESIUM STEARATE
POLYVINYL ALCOHOL, UNSPECIFIED
POLYETHYLENE GLYCOL, UNSPECIFIED
TITANIUM DIOXIDE
TALC
FERRIC OXIDE RED
FD&C YELLOW NO. 6
FD&C BLUE NO. 2
INDIGOTINDISULFONATE SODIUM
Product Characteristics
Color PINK Score no score
Shape ROUND Size 8mm
Flavor Imprint Code VS;80
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50436-2168-1 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090642 01/05/2015
Labeler — Unit Dose Services (831995316)
Establishment
Name Address ID/FEI Operations
Unit Dose Services 831995316 REPACK (50436-2168), RELABEL (50436-2168)

Revised: 06/2018 Unit Dose Services

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