FDA NDC Directory · JSON-LD · Markdown

DEFERIPRONE

NDC 75907-349 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Generic namedeferiprone
Labeler / ManufacturerDR. REDDY'S LABORATORIES, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA220132
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsDEFERIPRONE (500 mg/1)
Marketing started20251215
Package count1

External sources

Source: openFDA. Public-domain (CC0).