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Clopidogrel Bisulfate

NDC 47335-894 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090494
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCLOPIDOGREL BISULFATE (75 mg/1)
Marketing started20120518
Package count5

External sources

Source: openFDA. Public-domain (CC0).