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Hydralazine Hydrochloride

NDC 67877-291 · Ascend Laboratories, LLC

Generic nameHydralazine Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDRALAZINE HYDROCHLORIDE
Strength50 mg/1
Pharmacologic classArteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
Marketing categoryANDA

Packages

67877-291-01 — 100 TABLET in 1 BOTTLE (67877-291-01)

67877-291-05 — 500 TABLET in 1 BOTTLE (67877-291-05)

67877-291-10 — 1000 TABLET in 1 BOTTLE (67877-291-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

64380-734 — HydrALAZINE Hydrochloride, 64380-735 — HydrALAZINE Hydrochloride, 64380-736 — HydrALAZINE Hydrochloride, 67046-1517 — hydralazine hydrochloride, 67046-1520 — Hydralazine Hydrochloride, 67046-1609 — Hydralazine Hydrochloride, 67046-1660 — Hydralazine Hydrochloride, 67046-2080 — HydrALAZINE Hydrochloride, 67544-657 — Hydralazine Hydrochloride, 67877-290 — Hydralazine Hydrochloride, 67877-292 — Hydralazine Hydrochloride, 67877-293 — Hydralazine Hydrochloride, 68071-1940 — Hydralazine Hydrochloride, 68071-2055 — Hydralazine Hydrochloride, 68071-5285 — Hydralazine Hydrochloride, 68462-341 — Hydralazine Hydrochloride, 68462-342 — Hydralazine Hydrochloride, 68462-343 — Hydralazine Hydrochloride, 68462-344 — Hydralazine Hydrochloride, 68475-514 — Hydralazine Hydrochloride, +139 more

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