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OLMESARTAN MEDOXOMIL

NDC 0527-2425 · Lannett Company, Inc.

Generic nameOlmesartan medoxomil
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)OLMESARTAN MEDOXOMIL
Strength5 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

0527-2425-32 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-32)

0527-2425-46 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-46)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-5002 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0093-5003 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0093-5004 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0093-5005 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0093-5006 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0527-2426 — Olmesartan medoxomil, 0527-2427 — Olmesartan medoxomil, 0713-0860 — olmesartan medoxomil, 0713-0861 — olmesartan medoxomil, 0713-0862 — olmesartan medoxomil, 0713-0863 — olmesartan medoxomil-hydrochlorothiazide, 0713-0864 — olmesartan medoxomil-hydrochlorothiazide, 0713-0865 — olmesartan medoxomil-hydrochlorothiazide, 0713-0870 — amlodipine besylate and olmesartan medoxomil, 0713-0871 — amlodipine besylate and olmesartan medoxomil, 0713-0872 — amlodipine besylate and olmesartan medoxomil, 0713-0873 — amlodipine besylate and olmesartan medoxomil, 0713-0874 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 0713-0875 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 0713-0876 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, +281 more

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