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HYDRALAZINE HYDROCHLORIDE

NDC 71209-017 · Cadila Pharmaceuticals Limited

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

Packages

71209-017-05 — 100 TABLET in 1 BOTTLE (71209-017-05)

71209-017-11 — 1000 TABLET in 1 BOTTLE (71209-017-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-3659 — hydrALAZINE Hydrochloride, 70518-3852 — Hydralazine Hydrochloride, 70518-4007 — Hydralazine Hydrochloride, 70518-4022 — 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, 71209-018 — hydralazine hydrochloride, 71288-205 — HYDRALAZINE HYDROCHLORIDE, 71335-0202 — Hydralazine Hydrochloride, 71335-1589 — Hydralazine Hydrochloride, 71335-1685 — Hydralazine Hydrochloride, 71335-2307 — Hydralazine Hydrochloride, 71335-2352 — Hydralazine Hydrochloride, 71335-9722 — Hydralazine Hydrochloride, 71335-9756 — Hydralazine Hydrochloride, 71610-549 — 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.