Amlodipine besylate and Olmesartan medoxomil

NDC 27241-085 · Ajanta Pharma USA Inc.

Generic nameAmlodipine besylate and Olmesartan medoxomil

Dosage formTABLET

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE, OLMESARTAN MEDOXOMIL

Strength10; 20 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

27241-085-03 — 30 TABLET in 1 BOTTLE (27241-085-03)

27241-085-09 — 90 TABLET in 1 BOTTLE (27241-085-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

23155-921 — Amlodipine and Benazepril Hydrochloride, 23155-922 — Amlodipine and Benazepril Hydrochloride, 23155-923 — Amlodipine and Benazepril Hydrochloride, 23155-924 — Amlodipine and Benazepril Hydrochloride, 23155-925 — Amlodipine and Benazepril Hydrochloride, 24338-001 — telmisartan, amlodipine and indapamide, 24338-002 — telmisartan, amlodipine and indapamide, 24338-003 — telmisartan, amlodipine and indapamide, 27241-083 — Amlodipine besylate and Olmesartan medoxomil, 27241-084 — Amlodipine besylate and Olmesartan medoxomil, 27241-086 — Amlodipine besylate and Olmesartan medoxomil, 29300-396 — Amlodipine Besylate, 29300-397 — Amlodipine Besylate, 29300-398 — Amlodipine Besylate, 31722-445 — Amlodipine and Olmesartan Medoxomil, 31722-446 — Aamlodipine and Olmesartan Medoxomil, 31722-447 — Amlodipine and Olmesartan Medoxomil, 31722-448 — Amlodipine and Olmesartan Medoxomil, 31722-852 — OLMESARTAN MEDOXOMIL, 31722-853 — OLMESARTAN MEDOXOMIL, +720 more

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