Skip to main content

Hydralazine Hydrochloride

NDC 23155-834 · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

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

Packages

23155-834-01 — 100 TABLET in 1 BOTTLE (23155-834-01)

23155-834-10 — 1000 TABLET in 1 BOTTLE (23155-834-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0641-6231 — HydrALAZINE hydrochloride, 0904-7447 — Hydralazine Hydrochloride, 0904-7448 — Hydralazine Hydrochloride, 0904-7449 — Hydralazine Hydrochloride, 0904-7450 — Hydralazine Hydrochloride, 23155-001 — hydralazine hydrochloride, 23155-002 — hydralazine hydrochloride, 23155-003 — hydralazine hydrochloride, 23155-832 — Hydralazine Hydrochloride, 23155-833 — Hydralazine Hydrochloride, 23155-835 — Hydralazine Hydrochloride, 24338-010 — Hydralazine hydrochloride and Isosorbide dinitrate, 31722-519 — Hydralazine Hydrochloride, 31722-520 — Hydralazine Hydrochloride, 31722-521 — Hydralazine Hydrochloride, 31722-522 — Hydralazine Hydrochloride, 33342-374 — Hydralazine Hydrochloride, 33342-375 — Hydralazine Hydrochloride, 33342-376 — Hydralazine Hydrochloride, 33342-377 — 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.