Amlodipine and olmesartan Medoxomil

NDC 67877-501 · Ascend Laboratories, LLC

Generic nameAmlodipine and olmesartan Medoxomil

Dosage formTABLET

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE, OLMESARTAN MEDOXOMIL

Strength5; 40 mg/1; mg/1

Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Marketing categoryANDA

Packages

67877-501-30 — 30 TABLET in 1 BOTTLE (67877-501-30)

67877-501-90 — 90 TABLET in 1 BOTTLE (67877-501-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67877-198 — Amlodipine besylate, 67877-199 — Amlodipine besylate, 67877-445 — Olmesartan Medoxomil, 67877-446 — Olmesartan Medoxomil, 67877-447 — Olmesartan Medoxomil, 67877-451 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 67877-452 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 67877-453 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 67877-499 — Amlodipine and olmesartan Medoxomil, 67877-500 — Amlodipine and olmesartan Medoxomil, 67877-502 — Amlodipine and olmesartan Medoxomil, 67877-900 — Amlodipine besylate, 67877-901 — Amlodipine besylate, 67877-902 — Amlodipine besylate, 68001-130 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-131 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-132 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-133 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-134 — Amlodipine Besylate and Benazepril Hydrochloride, 68001-135 — Amlodipine Besylate and Benazepril Hydrochloride, +720 more

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