FDA NDC Directory · JSON-LD · Markdown

Afatinib

NDC 31722-781 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210750
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAFATINIB DIMALEATE (20 mg/1)
Marketing started20260714
Package count1

External sources

Source: openFDA. Public-domain (CC0).