"61919-007-90" National Drug Code (NDC)

NDC Code	61919-007-90
Package Description	90 TABLET, FILM COATED in 1 BOTTLE (61919-007-90)
Product NDC	61919-007
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Clopidogrel
Non-Proprietary Name	Clopidogrel
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20140101
Marketing Category Name	ANDA
Application Number	ANDA090540
Manufacturer	DIRECT RX
Substance Name	CLOPIDOGREL BISULFATE
Strength	75
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]