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Irinotecan hydrochloride

NDC 68083-382 · Gland Pharma Limited

Generic nameIrinotecan hydrochloride
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)IRINOTECAN HYDROCHLORIDE
Strength20 mg/mL
Pharmacologic classTopoisomerase Inhibitor [EPC], Topoisomerase Inhibitors [MoA]
Marketing categoryANDA

Packages

68083-382-01 — 1 VIAL, SINGLE-DOSE in 1 CARTON (68083-382-01) / 5 mL in 1 VIAL, SINGLE-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16714-131 — Irinotecan hydrochloride, 25021-230 — irinotecan hydrochloride, 45963-614 — Irinotecan hydrochloride, 50742-401 — Irinotecan Hydrochloride, 50742-402 — Irinotecan Hydrochloride, 55150-352 — IRINOTECAN HYDROCHLORIDE, 55150-353 — IRINOTECAN HYDROCHLORIDE, 55150-354 — IRINOTECAN HYDROCHLORIDE, 55150-355 — IRINOTECAN HYDROCHLORIDE, 60505-6128 — Irinotecan Hydrochloride, 60505-6272 — Irinotecan Hydrochloride, 61703-349 — Irinotecan Hydrochloride, 63323-193 — IRINOTECAN HYDROCHLORIDE, 67184-0511 — Irinotecan Hydrochloride, 67184-0512 — Irinotecan Hydrochloride, 67184-0513 — Irinotecan Hydrochloride, 68001-480 — Irinotecan hydrochloide, 68083-381 — Irinotecan hydrochloide, 70700-169 — Irinotecan hydrochloide, 70700-170 — Irinotecan hydrochloride, +8 more

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