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DOXORUBICIN HYDROCHLORIDE

NDC 68001-703 · BluePoint Laboratories

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

68001-703-36 — 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-703-36) / 10 mL in 1 VIAL, SINGLE-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68001-493 — Doxorubicin Hydrochloride, 68001-629 — 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, +43 more

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