Home > National Drug Code (NDC) > Clopidogrel Bisulfate

Clopidogrel Bisulfate - 55154-6278-9 - (clopidogrel)

Alphabetical Index


Drug Information of Clopidogrel Bisulfate

Product NDC: 55154-6278
Proprietary Name: Clopidogrel Bisulfate
Non Proprietary Name: clopidogrel
Active Ingredient(s): 75    mg/1 & nbsp;   clopidogrel
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Clopidogrel Bisulfate

Product NDC: 55154-6278
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077665
Marketing Category: ANDA
Start Marketing Date: 20120517

Package Information of Clopidogrel Bisulfate

Package NDC: 55154-6278-9
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (55154-6278-9)

NDC Information of Clopidogrel Bisulfate

NDC Code 55154-6278-9
Proprietary Name Clopidogrel Bisulfate
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (55154-6278-9)
Product NDC 55154-6278
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clopidogrel
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120517
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CLOPIDOGREL BISULFATE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA]

Complete Information of Clopidogrel Bisulfate


General Information