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HYDRALAZINE HYDROCHLORIDE

NDC 63629-5696 · Bryant Ranch Prepack

FDA lists marketing as ended on 2026-08-31.
Generic namehydralazine hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)HYDRALAZINE HYDROCHLORIDE
Strength25 mg/1
Pharmacologic classArteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
Marketing categoryANDA

Packages

63629-5696-1 — 30 TABLET, FILM COATED in 1 BOTTLE (63629-5696-1)

63629-5696-2 — 60 TABLET, FILM COATED in 1 BOTTLE (63629-5696-2)

63629-5696-3 — 90 TABLET, FILM COATED in 1 BOTTLE (63629-5696-3)

63629-5696-4 — 10 TABLET, FILM COATED in 1 BOTTLE (63629-5696-4)

63629-5696-5 — 100 TABLET, FILM COATED in 1 BOTTLE (63629-5696-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-811 — Hydralazine Hydrochloride, 60687-822 — Hydralazine Hydrochloride, 60687-833 — Hydralazine Hydrochloride, 62135-579 — Hydralazine Hydrochloride, 62135-580 — Hydralazine Hydrochloride, 62135-581 — Hydralazine Hydrochloride, 62135-582 — Hydralazine Hydrochloride, 63187-901 — Hydralazine Hydrochloride, 63323-614 — hydrALAZINE Hydrochloride, 63629-5246 — Hydralazine Hydrochloride, 63629-8493 — Hydralazine Hydrochloride, 63629-8494 — Hydralazine Hydrochloride, 63629-8495 — Hydralazine Hydrochloride, 63629-8496 — Hydralazine Hydrochloride, 63629-8497 — Hydralazine Hydrochloride, 63629-8757 — Hydralazine Hydrochloride, 64380-733 — HydrALAZINE Hydrochloride, 64380-734 — HydrALAZINE Hydrochloride, 64380-735 — HydrALAZINE Hydrochloride, 64380-736 — 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.