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Erlotinib

NDC 70771-1522 · Zydus Lifesciences 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

70771-1522-3 — 30 TABLET, FILM COATED in 1 BOTTLE (70771-1522-3)

70771-1522-7 — 3 BLISTER PACK in 1 CARTON (70771-1522-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1522-2)

70771-1522-9 — 90 TABLET, FILM COATED in 1 BOTTLE (70771-1522-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-565 — ERLOTINIB HYDROCHLORIDE, 46708-566 — ERLOTINIB HYDROCHLORIDE, 46708-567 — ERLOTINIB HYDROCHLORIDE, 59651-530 — Erlotinib, 59651-531 — 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, 70771-1523 — Erlotinib, 72205-080 — Erlotinib Hydrochloride, 72205-081 — Erlotinib Hydrochloride, 72205-082 — Erlotinib Hydrochloride, 72485-217 — Erlotinib hydrochloride, 72485-218 — Erlotinib hydrochloride, 72485-219 — Erlotinib hydrochloride, +6 more

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