Telmisartan

NDC 71209-049 · Cadila Pharmaceuticals Limited

Generic nameTelmisartan

Dosage formTABLET

RouteORAL

Active ingredient(s)TELMISARTAN

Strength20 mg/1

Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]

Marketing categoryANDA

Packages

71209-049-01 30 TABLET in 1 BOTTLE (71209-049-01)

71209-049-04 90 TABLET in 1 BOTTLE (71209-049-04)

71209-049-05 100 TABLET in 1 BOTTLE (71209-049-05)

71209-049-10 500 TABLET in 1 BOTTLE (71209-049-10)

71209-049-11 1000 TABLET in 1 BOTTLE (71209-049-11)

71209-049-16 30 BLISTER PACK in 1 CARTON (71209-049-16) / 10 TABLET in 1 BLISTER PACK

71209-049-18 30 BLISTER PACK in 1 CARTON (71209-049-18) / 10 TABLET in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

68788-8718 — telmisartan, 70518-2572 — Telmisartan, 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, 71209-050 — Telmisartan, 71209-051 — 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, +99 more

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