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Isosorbide dinitrate

NDC 70710-1151 · Zydus Pharmaceuticals (USA) Inc.

Generic nameIsosorbide dinitrate
Dosage formTABLET
RouteORAL
Active ingredient(s)ISOSORBIDE DINITRATE
Strength30 mg/1
Pharmacologic classNitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE]
Marketing categoryANDA

Packages

70710-1151-0 — 1000 TABLET in 1 BOTTLE (70710-1151-0)

70710-1151-1 — 100 TABLET in 1 BOTTLE (70710-1151-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68001-375 — Isosorbide Dinitrate, 68001-562 — Isosorbide dinitrate, 68084-082 — Isosorbide Dinitrate, 68084-083 — Isosorbide Dinitrate, 68682-192 — isosorbide dinitrate, 68682-193 — isosorbide dinitrate, 70518-4405 — isosorbide dinitrate, 70710-1148 — Isosorbide dinitrate, 70710-1149 — Isosorbide dinitrate, 70710-1150 — Isosorbide dinitrate, 70710-1152 — Isosorbide dinitrate, 70771-1501 — Isosorbide dinitrate, 70771-1502 — Isosorbide dinitrate, 70771-1503 — Isosorbide dinitrate, 70771-1504 — Isosorbide dinitrate, 70771-1505 — Isosorbide dinitrate, 72162-2343 — hydralazine hydrochloride and isosorbide dinitrate, 72319-012 — isosorbide dinitrate and hydralazine hydrochloride, 72888-081 — isosorbide dinitrate, 72888-082 — isosorbide dinitrate, +40 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.