AMLODIPINE AND OLMESARTAN MEDOXOMIL

NDC 42571-236 · Micro Labs Limited

Generic nameAmlodipine 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

42571-236-05 — 500 TABLET in 1 BOTTLE (42571-236-05)

42571-236-10 — 1000 TABLET in 1 BOTTLE (42571-236-10)

42571-236-30 — 30 TABLET in 1 BOTTLE (42571-236-30)

42571-236-90 — 90 TABLET in 1 BOTTLE (42571-236-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42291-003 — Amlodipine and Olmesartan Medoxomil, 42291-004 — Amlodipine and Olmesartan Medoxomil, 42291-015 — Amlodipine and Benazepril Hydrochloride, 42291-025 — Amlodipine Besylate, 42291-026 — Amlodipine Besylate, 42291-027 — Amlodipine Besylate, 42291-924 — olmesartan medoxomil-hydrochlorothiazide, 42291-925 — olmesartan medoxomil-hydrochlorothiazide, 42291-926 — olmesartan medoxomil-hydrochlorothiazide, 42571-235 — Amlodipine and Olmesartan Medoxomil, 42571-237 — Amlodipine and Olmesartan Medoxomil, 42571-238 — Amlodipine and Olmesartan Medoxomil, 42571-245 — Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide, 42571-246 — Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide, 42571-247 — Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide, 42571-248 — Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide, 42571-249 — Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide, 42708-066 — Amlodipine besylate, 42806-055 — AMLODIPINE BESYLATE, 42806-056 — AMLODIPINE BESYLATE, +720 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels