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Clopidogrel bisulfate

NDC 77771-121 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerRADHA PHARMACEUTICALS, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204165
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCLOPIDOGREL BISULFATE (300 mg/1)
Marketing started20230220
Package count3

External sources

Source: openFDA. Public-domain (CC0).