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telmisartan

NDC 68382-473 · Zydus Pharmaceuticals USA Inc.

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

68382-473-01 — 100 TABLET in 1 BOTTLE (68382-473-01)

68382-473-05 — 500 TABLET in 1 BOTTLE (68382-473-05)

68382-473-06 — 30 TABLET in 1 BOTTLE (68382-473-06)

68382-473-10 — 1000 TABLET in 1 BOTTLE (68382-473-10)

68382-473-16 — 90 TABLET in 1 BOTTLE (68382-473-16)

68382-473-78 — 30 BLISTER PACK in 1 CARTON (68382-473-78) / 1 TABLET in 1 BLISTER PACK (68382-473-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67877-484 — telmisartan, 68071-3892 — Telmisartan, 68071-5178 — Telmisartan, 68180-193 — Telmisartan and Hydrochlorothiazide, 68180-194 — Telmisartan and Hydrochlorothiazide, 68180-195 — Telmisartan and Hydrochlorothiazide, 68180-196 — Telmisartan and Amlodipine, 68180-197 — Telmisartan and Amlodipine, 68382-471 — telmisartan, 68382-472 — 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, 68788-8665 — 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.