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Benicar

NDC 0713-0942 · Cosette Pharmaceuticals, Inc.

Generic nameolmesartan medoxomil
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)OLMESARTAN MEDOXOMIL
Strength40 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryNDA

Packages

0713-0942-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0942-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 0713-0877 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 0713-0878 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 0713-0940 — olmesartan medoxomil, 0713-0941 — olmesartan medoxomil, 0713-0943 — olmesartan medoxomil-hydrochlorothiazide, 0713-0944 — olmesartan medoxomil-hydrochlorothiazide, 0713-0945 — olmesartan medoxomil-hydrochlorothiazide, 16729-320 — olmesartan medoxomil, 16729-321 — olmesartan medoxomil, 16729-322 — olmesartan medoxomil, 16729-366 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 16729-367 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 16729-368 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 27241-083 — Amlodipine besylate and Olmesartan medoxomil, +281 more

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