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Telmisartan

NDC 33342-118 · Macleods 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

33342-118-07 — 30 TABLET in 1 CONTAINER (33342-118-07)

33342-118-10 — 90 TABLET in 1 CONTAINER (33342-118-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0378-1078 — telmisartan and amlodipine, 0378-2920 — telmisartan, 0378-2921 — telmisartan, 0378-2922 — telmisartan, 0597-0042 — telmisartan and hydrochlorothiazide, 0597-0043 — telmisartan and hydrochlorothiazide, 0597-0044 — telmisartan and hydrochlorothiazide, 24338-001 — telmisartan, amlodipine and indapamide, 24338-002 — telmisartan, amlodipine and indapamide, 24338-003 — telmisartan, amlodipine and indapamide, 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, +99 more

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