Telmisartan

NDC 50090-5492 · A-S Medication Solutions

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

50090-5492-0 — 90 TABLET in 1 BOTTLE, PLASTIC (50090-5492-0)

FDA lists these products with the same active ingredient.

46708-185 — Telmisartan and Amlodipine, 46708-186 — Telmisartan and Amlodipine, 46708-187 — Telmisartan and Amlodipine, 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, 53746-291 — Telmisartan, 53746-292 — Telmisartan, 53746-293 — Telmisartan, 59746-439 — Telmisartan, 59746-440 — Telmisartan, 59746-441 — Telmisartan, 62135-535 — TELMISARTAN, 62135-536 — TELMISARTAN, 62135-537 — TELMISARTAN, 62332-087 — 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.