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"68084-752-19" National Drug Code (NDC)

Clopidogrel 20 BLISTER PACK in 1 CARTON (68084-752-19) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-752-18)
(American Health Packaging)

NDC Code68084-752-19
Package Description20 BLISTER PACK in 1 CARTON (68084-752-19) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-752-18)
Product NDC68084-752
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameClopidogrel
Non-Proprietary NameClopidogrel Bisulfate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140328
Marketing Category NameANDA
Application NumberANDA076274
ManufacturerAmerican Health Packaging
Substance NameCLOPIDOGREL BISULFATE
Strength300
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]

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