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OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

NDC 70518-4517 · REMEDYREPACK INC.

Generic nameOLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)OLMESARTAN MEDOXOMIL, HYDROCHLOROTHIAZIDE
Strength12.5; 40 mg/1; mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

70518-4517-0 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4517-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4053 — olmesartan medoxomil, 70518-4113 — Hydrochlorothiazide, 70518-4165 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 70518-4251 — hydrochlorothiazide, 70518-4270 — Triamterene and Hydrochlorothiazide, 70518-4316 — olmesartan medoxomil, 70518-4351 — Triamterene and Hydrochlorothiazide, 70518-4359 — hydrochlorothiazide, 70518-4466 — HYDROCHLOROTHIAZIDE, 70518-4516 — Lisinopril and Hydrochlorothiazide Tablets, 70518-4525 — hydrochlorothiazide, 70518-4577 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 70518-4598 — Olmesartan medoxomil, 70756-315 — telmisartan and hydrochlorothiazide, 70756-316 — telmisartan and hydrochlorothiazide, 70756-317 — telmisartan and hydrochlorothiazide, 70756-808 — OLMESARTAN MEDOXOMIL, 70756-809 — OLMESARTAN MEDOXOMIL, 70756-810 — OLMESARTAN MEDOXOMIL, 70756-812 — Olmesartan Medoxomil and Hydrochlorothiazide, +1040 more

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