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Hydralazine Hydrochloride

NDC 70518-4022 · REMEDYREPACK INC.

Generic nameHydralazine Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDRALAZINE HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classArteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
Marketing categoryANDA

Packages

70518-4022-0 — 30 TABLET in 1 BLISTER PACK (70518-4022-0)

70518-4022-1 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-4022-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68462-341 — Hydralazine Hydrochloride, 68462-342 — Hydralazine Hydrochloride, 68462-343 — Hydralazine Hydrochloride, 68462-344 — Hydralazine Hydrochloride, 68475-514 — Hydralazine Hydrochloride, 68788-8087 — Hydralazine Hydrochloride, 70518-2551 — Hydralazine Hydrochloride, 70518-3659 — hydrALAZINE Hydrochloride, 70518-3852 — Hydralazine Hydrochloride, 70518-4007 — Hydralazine Hydrochloride, 70518-4064 — Hydralazine Hydrochloride, 70518-4352 — Hydralazine Hydrochloride, 70710-1988 — Hydralazine Hydrochloride, 71205-072 — HydrALAZINE Hydrochloride, 71205-091 — Hydralazine Hydrochloride, 71209-016 — hydralazine hydrochloride, 71209-017 — hydralazine hydrochloride, 71209-018 — hydralazine hydrochloride, 71288-205 — HYDRALAZINE HYDROCHLORIDE, 71335-0202 — 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.