telmisartan

NDC 65841-806 · Zydus Lifesciences Limited

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

65841-806-01 — 100 TABLET in 1 BOTTLE (65841-806-01)

65841-806-05 — 500 TABLET in 1 BOTTLE (65841-806-05)

65841-806-06 — 30 TABLET in 1 BOTTLE (65841-806-06)

65841-806-10 — 1000 TABLET in 1 BOTTLE (65841-806-10)

65841-806-16 — 90 TABLET in 1 BOTTLE (65841-806-16)

65841-806-78 — 30 BLISTER PACK in 1 CARTON (65841-806-78) / 1 TABLET in 1 BLISTER PACK (65841-806-30)

FDA lists these products with the same active ingredient.

62332-209 — Telmisartan and Hydrochlorothiazide, 62332-210 — Telmisartan and Hydrochlorothiazide, 62332-211 — Telmisartan and Hydrochlorothiazide, 63187-951 — telmisartan, 63629-5682 — telmisartan, 65162-291 — Telmisartan, 65162-292 — Telmisartan, 65162-293 — Telmisartan, 65841-804 — telmisartan, 65841-805 — telmisartan, 65862-867 — Telmisartan, 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, +99 more

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