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Raloxifene Hydrochloride

NDC 65862-709 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204310
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRALOXIFENE HYDROCHLORIDE (60 mg/1)
Marketing started20150828
Package count5

External sources

Source: openFDA. Public-domain (CC0).