Telmisartan

NDC 72603-832 · NorthStar RxLLC

Generic nameTelmisartan

Dosage formTABLET

RouteORAL

Active ingredient(s)TELMISARTAN

Strength40 mg/1

Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]

Marketing categoryANDA

Packages

72603-832-01 — 30 TABLET in 1 CONTAINER (72603-832-01)

FDA lists these products with the same active ingredient.

70756-314 — Telmisartan, 70756-315 — telmisartan and hydrochlorothiazide, 70756-316 — telmisartan and hydrochlorothiazide, 70756-317 — telmisartan and hydrochlorothiazide, 71209-049 — Telmisartan, 71209-050 — Telmisartan, 71209-051 — Telmisartan, 71335-1428 — telmisartan, 71335-1723 — Telmisartan, 71335-2173 — Telmisartan, 71335-2191 — Telmisartan, 72162-2438 — Telmisartan, 72162-2439 — Telmisartan, 72162-2440 — Telmisartan, 72241-015 — Telmisartan, 72241-016 — Telmisartan, 72241-017 — Telmisartan, 72603-831 — Telmisartan, 72603-833 — Telmisartan, 72789-371 — telmisartan, +99 more

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