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Hydralazine Hydrochloride

NDC 60687-822 · American Health Packaging

Generic nameHydralazine Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDRALAZINE HYDROCHLORIDE
Strength25 mg/1
Pharmacologic classArteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
Marketing categoryANDA

Packages

60687-822-01 — 100 BLISTER PACK in 1 CARTON (60687-822-01) / 1 TABLET in 1 BLISTER PACK (60687-822-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-0186 — Hydralazine Hydrochloride, 55154-0187 — Hydralazine Hydrochloride, 55154-2140 — Hydralazine Hydrochloride, 55154-2141 — Hydralazine Hydrochloride, 55154-5085 — Hydralazine Hydrochloride, 55154-5689 — Hydralazine Hydrochloride, 55154-9554 — HYDRALAZINE HYDROCHLORIDE, 55154-9587 — HYDRALAZINE HYDROCHLORIDE, 55289-133 — hydralazine hydrochloride, 60687-811 — 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, 63629-5696 — hydralazine hydrochloride, 63629-8493 — 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.