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Telmisartan

NDC 43547-285 · Solco Healthcare US, LLC

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

43547-285-03 — 30 TABLET in 1 BOTTLE (43547-285-03)

43547-285-09 — 90 TABLET in 1 BOTTLE (43547-285-09)

43547-285-50 — 500 TABLET in 1 BOTTLE (43547-285-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

33342-119 — Telmisartan, 33342-120 — Telmisartan, 42291-462 — Telmisartan and Hydrochlorothiazide, 42291-463 — Telmisartan and Hydrochlorothiazide, 42291-464 — Telmisartan and Hydrochlorothiazide, 42291-790 — Telmisartan, 42291-791 — Telmisartan, 42291-792 — Telmisartan, 43547-283 — Telmisartan, 43547-284 — Telmisartan, 43547-441 — telmisartan and hydrochlorothiazide, 43547-442 — telmisartan and hydrochlorothiazide, 43547-443 — telmisartan and hydrochlorothiazide, 46708-184 — Telmisartan and Amlodipine, 46708-185 — Telmisartan and Amlodipine, 46708-186 — Telmisartan and Amlodipine, 46708-187 — Telmisartan and Amlodipine, 46708-209 — Telmisartan and Hydrochlorothiazide, 46708-210 — Telmisartan and Hydrochlorothiazide, 46708-211 — 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.