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Clopidogrel

NDC 68071-4023 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameClopidogrel Bisulfate
Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090540
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCLOPIDOGREL BISULFATE (75 mg/1)
Marketing started20120517
Package count1

External sources

Source: openFDA. Public-domain (CC0).