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Telmisartan

NDC 65162-293 · Amneal Pharmaceuticals 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

65162-293-03 — 30 TABLET in 1 BOTTLE (65162-293-03)

65162-293-09 — 90 TABLET in 1 BOTTLE (65162-293-09)

65162-293-11 — 1000 TABLET in 1 BOTTLE (65162-293-11)

65162-293-50 — 500 TABLET in 1 BOTTLE (65162-293-50)

65162-293-63 — 3 BLISTER PACK in 1 CARTON (65162-293-63) / 10 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62332-087 — Telmisartan, 62332-088 — Telmisartan, 62332-089 — Telmisartan, 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, 65841-804 — telmisartan, 65841-805 — telmisartan, 65841-806 — 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, +99 more

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