FDA NDC Directory · JSON-LD · Markdown

Gefitinib

NDC 50742-366 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerIngenus Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211591
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsGEFITINIB (250 mg/1)
Marketing started20230427
Package count1

External sources

Source: openFDA. Public-domain (CC0).