Telmisartan

NDC 68071-5178 · NuCare Pharmaceuticals,Inc.

Generic nameTelmisartan

Dosage formTABLET

RouteORAL

Active ingredient(s)TELMISARTAN

Strength80 mg/1

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

Marketing categoryANDA

Packages

68071-5178-3 — 30 TABLET in 1 BOX (68071-5178-3)

FDA lists these products with the same active ingredient.

65862-868 — Telmisartan, 65862-869 — Telmisartan, 65862-976 — Telmisartan and Hydrochlorothiazide, 65862-977 — Telmisartan and Hydrochlorothiazide, 65862-978 — Telmisartan and Hydrochlorothiazide, 67296-2284 — Telmisartan, 67877-482 — telmisartan, 67877-483 — telmisartan, 67877-484 — telmisartan, 68071-3892 — Telmisartan, 68180-193 — Telmisartan and Hydrochlorothiazide, 68180-194 — Telmisartan and Hydrochlorothiazide, 68180-195 — Telmisartan and Hydrochlorothiazide, 68180-196 — Telmisartan and Amlodipine, 68180-197 — Telmisartan and Amlodipine, 68382-471 — telmisartan, 68382-472 — telmisartan, 68382-473 — telmisartan, 68462-199 — Telmisartan, 68462-200 — Telmisartan, +99 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.