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Raloxifene Hydrochloride

NDC 76282-256 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerExelan Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090842
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRALOXIFENE HYDROCHLORIDE (60 mg/1)
Marketing started20141112
Package count5

External sources

Source: openFDA. Public-domain (CC0).