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Raloxifene hydrochloride

NDC 50090-6177 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA211324
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsRALOXIFENE HYDROCHLORIDE (60 mg/1)
Marketing started20171230
Package count1

External sources

Source: openFDA. Public-domain (CC0).