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Telmisartan

NDC 71209-051 · Cadila Pharmaceuticals 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

71209-051-01 30 TABLET in 1 BOTTLE (71209-051-01)

71209-051-04 90 TABLET in 1 BOTTLE (71209-051-04)

71209-051-05 100 TABLET in 1 BOTTLE (71209-051-05)

71209-051-10 500 TABLET in 1 BOTTLE (71209-051-10)

71209-051-11 1000 TABLET in 1 BOTTLE (71209-051-11)

71209-051-16 30 BLISTER PACK in 1 CARTON (71209-051-16) / 10 TABLET in 1 BLISTER PACK

71209-051-18 30 BLISTER PACK in 1 CARTON (71209-051-18) / 10 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-3556 — Telmisartan, 70518-3798 — telmisartan, 70756-312 — Telmisartan, 70756-313 — Telmisartan, 70756-314 — Telmisartan, 70756-315 — telmisartan and hydrochlorothiazide, 70756-316 — telmisartan and hydrochlorothiazide, 70756-317 — telmisartan and hydrochlorothiazide, 71209-049 — Telmisartan, 71209-050 — Telmisartan, 71335-1428 — telmisartan, 71335-1723 — Telmisartan, 71335-2173 — Telmisartan, 71335-2191 — Telmisartan, 72162-2438 — Telmisartan, 72162-2439 — Telmisartan, 72162-2440 — Telmisartan, 72241-015 — Telmisartan, 72241-016 — Telmisartan, 72241-017 — 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.