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OLMESARTAN MEDOXOMIL, AMLODIPINE and HYDROCHLOROTHIAZIDE

NDC 42571-246 · Micro Labs Limited

Generic nameOlmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)OLMESARTAN MEDOXOMIL, AMLODIPINE BESYLATE, HYDROCHLOROTHIAZIDE
Strength5; 12.5; 40 mg/1; 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], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

42571-246-05 — 500 TABLET, FILM COATED in 1 BOTTLE (42571-246-05)

42571-246-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (42571-246-10)

42571-246-30 — 30 TABLET, FILM COATED in 1 BOTTLE (42571-246-30)

42571-246-90 — 90 TABLET, FILM COATED in 1 BOTTLE (42571-246-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42291-966 — Valsartan and Hydrochlorothiazide, 42291-967 — Valsartan and Hydrochlorothiazide, 42291-968 — Valsartan and Hydrochlorothiazide, 42291-969 — Valsartan and Hydrochlorothiazide, 42292-017 — spironolactone and hydrochlorothiazide, 42571-235 — Amlodipine and Olmesartan Medoxomil, 42571-236 — Amlodipine and Olmesartan Medoxomil, 42571-237 — Amlodipine and Olmesartan Medoxomil, 42571-238 — Amlodipine and Olmesartan Medoxomil, 42571-245 — Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide, 42571-247 — Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide, 42571-248 — Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide, 42571-249 — Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide, 42708-027 — Hydrochlorothiazide, 42708-028 — Hydrochlorothiazide, 42708-034 — Lisinopril and Hydrochlorothiazide, 42708-036 — Losartan Potassium and Hydrochlorothiazide, 42708-066 — Amlodipine besylate, 42708-079 — Hydrochlorothiazide, 42708-086 — hydrochlorothiazide, +1450 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