Telmisartan

NDC 53746-293 · Amneal Pharmaceuticals of New York LLC

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

53746-293-30 — 30 TABLET in 1 BOTTLE (53746-293-30)

FDA lists these products with the same active ingredient.

46708-209 — Telmisartan and Hydrochlorothiazide, 46708-210 — Telmisartan and Hydrochlorothiazide, 46708-211 — Telmisartan and Hydrochlorothiazide, 46708-608 — Telmisartan, 46708-609 — Telmisartan, 46708-610 — Telmisartan, 50090-5490 — telmisartan, 50090-5492 — telmisartan, 53746-291 — Telmisartan, 53746-292 — Telmisartan, 59746-439 — Telmisartan, 59746-440 — Telmisartan, 59746-441 — Telmisartan, 62135-535 — TELMISARTAN, 62135-536 — TELMISARTAN, 62135-537 — TELMISARTAN, 62332-087 — Telmisartan, 62332-088 — Telmisartan, 62332-089 — Telmisartan, 62332-209 — Telmisartan and Hydrochlorothiazide, +99 more

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