FDA NDC Directory · JSON-LD · Markdown

Deferasirox

NDC 69238-1487 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210727
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDEFERASIROX (180 mg/1)
Marketing started20200615
Package count1

External sources

Source: openFDA. Public-domain (CC0).