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DEFERASIROX

NDC 46708-412 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211824
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDEFERASIROX (360 mg/1)
Marketing started20191121
Package count2

External sources

Source: openFDA. Public-domain (CC0).