olmesartan medoxomil

NDC 63629-8525 · Bryant Ranch Prepack

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 categoryANDA

Packages

63629-8525-1 — 30 TABLET, FILM COATED in 1 BOTTLE (63629-8525-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62332-214 — Amlodipine besylate and Olmesartran medoxomil, 62332-215 — Amlodipine besylate and Olmesartran medoxomil, 63629-2238 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 63629-2239 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 63629-2240 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 63629-2241 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 63629-4307 — Olmesartan Medoxomil and Hydrochlorothiazide, 63629-8522 — olmesartan medoxomil, 63629-8523 — olmesartan medoxomil, 63629-8524 — olmesartan medoxomil, 63629-9426 — olmesartan medoxomil, 64980-602 — olmesartan medoxomil, 64980-603 — olmesartan medoxomil, 64980-665 — olmesartan medoxomil, 65862-741 — Olmesartan Medoxomil, 65862-742 — Olmesartan Medoxomil, 65862-743 — Olmesartan Medoxomil, 65862-779 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-780 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-781 — Olmesartan Medoxomil and Hydrochlorothiazide, +281 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.