Clopidogrel Bisulfate (Page 7 of 7)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 75 mg (30 tablet Bottle)

63187-639-30

75 mg

63187-639-30
(click image for full-size original)
CLOPIDOGREL BISULFATE clopidogrel bisulfate tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63187-639(NDC:50228-124)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Clopidogrel bisulfate (Clopidogrel) Clopidogrel 75 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM
HYDROGENATED CASTOR OIL
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
MANNITOL
MICROCRYSTALLINE CELLULOSE
HYPROMELLOSE, UNSPECIFIED
FERRIC OXIDE RED
POLYETHYLENE GLYCOL 400
TITANIUM DIOXIDE
Product Characteristics
Color PINK Score no score
Shape ROUND Size 9mm
Flavor Imprint Code SG;124
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63187-639-30 30 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:63187-639-60 60 TABLET, FILM COATED in 1 BOTTLE None
3 NDC:63187-639-90 90 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA204165 04/01/2014
Labeler — Proficient Rx LP (079196022)
Establishment
Name Address ID/FEI Operations
Proficient Rx LP 079196022 REPACK (63187-639), RELABEL (63187-639)

Revised: 11/2019 Proficient Rx LP

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