Gefitinib

NDC 0480-4053 · Teva Pharmaceuticals, Inc.

Generic nameGefitinib

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)GEFITINIB

Strength250 mg/1

Pharmacologic classKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

Marketing categoryANDA

Packages

0480-4053-56 — 30 TABLET, FILM COATED in 1 BOTTLE (0480-4053-56)

FDA lists these products with the same active ingredient.

0310-0482 — Gefitinib, 50742-366 — Gefitinib, 67184-0531 — Gefitinib, 69339-168 — Gefitinib

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.