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Raloxifene Hydrochloride

NDC 69097-825 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameRaloxifene
Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090842
Dosage form / routeTABLET · ORAL
Active ingredientsRALOXIFENE HYDROCHLORIDE (60 mg/1)
Marketing started20160629
Package count3

External sources

Source: openFDA. Public-domain (CC0).