Clopidogrel Bisulfate (Page 7 of 7)

Clopidogrel

Label ImageLabel Image
CLOPIDOGREL BISULFATE clopidogrel bisulfate tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68151-3118(NDC:55111-196)
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
SILICON DIOXIDE
Croscarmellose Sodium
magnesium stearate
Mannitol
CELLULOSE, MICROCRYSTALLINE
HYPROMELLOSE 2910 (5 MPA.S)
Polyethylene glycol 400
titanium dioxide
Product Characteristics
Color WHITE Score no score
Shape ROUND Size 11mm
Flavor Imprint Code R;196
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68151-3118-9 1 TABLET, FILM COATED in 1 PACKAGE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076273 05/17/2012
Labeler — Carilion Materials Management (079239644)
Establishment
Name Address ID/FEI Operations
Carilion Materials Management 079239644 REPACK (68151-3118)

Revised: 08/2016 Carilion Materials Management

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