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Erlotinib

NDC 59651-531 · Aurobindo Pharma Limited

Generic nameErlotinib
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ERLOTINIB HYDROCHLORIDE
Strength100 mg/1
Pharmacologic classKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]
Marketing categoryANDA

Packages

59651-531-03 — 30 TABLET, FILM COATED in 1 BOTTLE (59651-531-03)

59651-531-10 — 1 BLISTER PACK in 1 CARTON (59651-531-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-7662 — Erlotinib, 0093-7663 — Erlotinib, 0093-7664 — Erlotinib, 31722-263 — ERLOTINIB, 31722-264 — ERLOTINIB, 31722-265 — ERLOTINIB, 46708-565 — ERLOTINIB HYDROCHLORIDE, 46708-566 — ERLOTINIB HYDROCHLORIDE, 46708-567 — ERLOTINIB HYDROCHLORIDE, 59651-530 — Erlotinib, 59651-532 — Erlotinib, 62332-565 — ERLOTINIB HYDROCHLORIDE, 62332-566 — ERLOTINIB HYDROCHLORIDE, 62332-567 — ERLOTINIB HYDROCHLORIDE, 68382-913 — Erlotinib, 68382-914 — Erlotinib, 68382-915 — Erlotinib, 70771-1521 — Erlotinib, 70771-1522 — Erlotinib, 70771-1523 — Erlotinib, +6 more

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