FDA NDC Directory · JSON-LD · Markdown

DEFERASIROX

NDC 59651-412 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214474
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDEFERASIROX (360 mg/1)
Marketing started20231016
Package count1

External sources

Source: openFDA. Public-domain (CC0).