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DOXORUBICIN HYDROCHLORIDE

NDC 49315-008 · Zydus Lifesciences Limited

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

Packages

49315-008-03 — 1 VIAL, SINGLE-DOSE in 1 CARTON (49315-008-03) / 10 mL in 1 VIAL, SINGLE-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0338-9581 — doxorubicin hydrochloride, 0338-9665 — doxorubicin hydrochloride, 0338-9667 — doxorubicin hydrochloride, 25021-207 — doxorubicin hydrochloride, 25021-263 — Doxorubicin Hydrochloride, 45963-733 — Doxorubicin hydrochloride, 46708-525 — doxorubicin hydrochloride, 46708-810 — doxorubicin hydrochloride, 47335-049 — Doxorubicin Hydrochloride, 47335-050 — Doxorubicin Hydrochloride, 49315-009 — doxorubicin hydrochloride, 62332-525 — doxorubicin hydrochloride, 62332-810 — doxorubicin hydrochloride, 62756-826 — DOXOrubicin Hydrochloride, 62756-827 — DOXOrubicin Hydrochloride, 63323-101 — DOXORUBICIN HYDROCHLORIDE, 63323-883 — DOXORUBICIN HYDROCHLORIDE, 67457-436 — Doxorubicin Hydrochloride, 68001-345 — Doxorubicin Hydrochloride, 68001-492 — 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.