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Telmisartan

NDC 65862-869 · Aurobindo Pharma 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

65862-869-03 — 3 BLISTER PACK in 1 CARTON (65862-869-03) / 10 TABLET in 1 BLISTER PACK (65862-869-10)

65862-869-30 — 30 TABLET in 1 BOTTLE (65862-869-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-951 — telmisartan, 63629-5682 — telmisartan, 65162-291 — Telmisartan, 65162-292 — Telmisartan, 65162-293 — Telmisartan, 65841-804 — telmisartan, 65841-805 — telmisartan, 65841-806 — telmisartan, 65862-867 — Telmisartan, 65862-868 — 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, 68071-5178 — Telmisartan, 68180-193 — Telmisartan and Hydrochlorothiazide, +99 more

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