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DOXORUBICIN HYDROCHLORIDE

NDC 70748-339 · Lupin Pharmaceuticals, Inc.

Generic nameDOXORUBICIN HYDROCHLORIDE
Dosage formINJECTION, SUSPENSION, LIPOSOMAL
RouteINTRAVENOUS
Active ingredient(s)DOXORUBICIN HYDROCHLORIDE
Strength2 mg/mL
Pharmacologic classAnthracycline Topoisomerase Inhibitor [EPC], Anthracyclines [CS], Topoisomerase Inhibitors [MoA]
Marketing categoryANDA

Packages

70748-339-01 — 1 VIAL, SINGLE-USE in 1 CARTON (70748-339-01) / 10 mL in 1 VIAL, SINGLE-USE

Billed under HCPCS

Q2050 — Injection, doxorubicin hydrochloride, liposomal, not otherwise specified, 10 mg Medicare Part B payment limit (ASP + 6%): $116.61

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68001-345 — Doxorubicin Hydrochloride, 68001-492 — Doxorubicin Hydrochloride, 68001-493 — Doxorubicin Hydrochloride, 68001-629 — DOXORUBICIN HYDROCHLORIDE, 68001-703 — doxorubicin hydrochloride, 68001-704 — doxorubicin hydrochloride, 68001-706 — doxorubicin hydrochloride, 68001-707 — doxorubicin hydrochloride, 68083-248 — Doxorubicin Hydrochloride, 68083-249 — Doxorubicin Hydrochloride, 68083-250 — Doxorubicin Hydrochloride, 70121-1218 — Doxorubicin, 70121-1219 — Doxorubicin Hydrochloride, 70710-1530 — doxorubicin hydrochloride, 70710-1531 — doxorubicin hydrochloride, 70748-340 — DOXORUBICIN HYDROCHLORIDE, 72603-103 — Doxorubicin Hydrochloride, 72603-200 — Doxorubicin Hydrochloride, 75907-363 — doxorubicin hydrochloride, 75907-364 — doxorubicin hydrochloride, +43 more

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