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Telmisartan

NDC 68788-8665 · Preferred Pharmaceuticals Inc.

Generic nameTelmisartan
Dosage formTABLET
RouteORAL
Active ingredient(s)TELMISARTAN
Strength40 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

68788-8665-3 — 30 TABLET in 1 BOTTLE (68788-8665-3)

68788-8665-6 — 60 TABLET in 1 BOTTLE (68788-8665-6)

68788-8665-9 — 90 TABLET in 1 BOTTLE (68788-8665-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68382-473 — telmisartan, 68462-199 — Telmisartan, 68462-200 — Telmisartan, 68462-201 — Telmisartan, 68462-840 — Telmisartan and Hydrochlorothiazide, 68462-841 — Telmisartan and Hydrochlorothiazide, 68462-842 — Telmisartan and Hydrochlorothiazide, 68788-4034 — Telmisartan, 68788-8440 — telmisartan, 68788-8441 — telmisartan, 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, +99 more

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