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Isosorbide Dinitrate

NDC 0781-1695 · Sandoz Inc.

Generic nameIsosorbide Dinitrate
Dosage formTABLET
RouteORAL
Active ingredient(s)ISOSORBIDE DINITRATE
Strength20 mg/1
Pharmacologic classNitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE]
Marketing categoryANDA

Packages

0781-1695-01 — 100 TABLET in 1 BOTTLE (0781-1695-01)

0781-1695-10 — 1000 TABLET in 1 BOTTLE (0781-1695-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-1769 — Isosorbide Dinitrate, 0143-1771 — Isosorbide Dinitrate, 0143-1772 — Isosorbide Dinitrate, 0615-8463 — isosorbide dinitrate, 0615-8464 — isosorbide dinitrate, 0615-8465 — isosorbide dinitrate, 0781-1556 — Isosorbide Dinitrate, 0781-1635 — Isosorbide Dinitrate, 0904-6619 — Isosorbide Dinitrate, 0904-6620 — Isosorbide Dinitrate, 16714-007 — Isosorbide dinitrate, 16714-008 — Isosorbide dinitrate, 16714-009 — Isosorbide dinitrate, 16714-010 — Isosorbide dinitrate, 24338-010 — Hydralazine hydrochloride and Isosorbide dinitrate, 49884-009 — isosorbide dinitrate, 49884-020 — isosorbide dinitrate, 49884-021 — isosorbide dinitrate, 49884-022 — isosorbide dinitrate, 49884-556 — 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.