"57237-189-30" National Drug Code (NDC)

NDC Code	57237-189-30
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (57237-189-30)
Product NDC	57237-189
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Clopidogrel
Non-Proprietary Name	Clopidogrel Bisulfate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20120517
Marketing Category Name	ANDA
Application Number	ANDA090540
Manufacturer	Citron Pharma LLC
Substance Name	CLOPIDOGREL BISULFATE
Strength	75
Strength Unit	mg/1
Pharmacy Classes	Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA],Cytochrome P450 2C8 Inhibitors [MoA]