"68071-4138-3" National Drug Code (NDC)

Clopidogrel 30 TABLET, FILM COATED in 1 BOTTLE (68071-4138-3)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-4138-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68071-4138-3)
Product NDC68071-4138
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameClopidogrel
Non-Proprietary NameClopidogrel
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120517
Marketing Category NameANDA
Application NumberANDA076999
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameCLOPIDOGREL BISULFATE
Strength75
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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