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bicalutamide

NDC 82804-082 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA079110
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBICALUTAMIDE (50 mg/1)
Marketing started20141215
Package count1

External sources

Source: openFDA. Public-domain (CC0).