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Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide

NDC 0093-5003 · Teva Pharmaceuticals USA, Inc.

Generic nameOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)OLMESARTAN MEDOXOMIL, AMLODIPINE BESYLATE, HYDROCHLOROTHIAZIDE
Strength10; 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

0093-5003-56 — 30 TABLET, FILM COATED in 1 BOTTLE (0093-5003-56)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0078-0491 — amlodipine besylate and valsartan, 0078-0559 — amlodipine valsartan and hydrochlorothiazide, 0078-0560 — amlodipine valsartan and hydrochlorothiazide, 0078-0561 — amlodipine valsartan and hydrochlorothiazide, 0078-0562 — amlodipine valsartan and hydrochlorothiazide, 0078-0563 — amlodipine valsartan and hydrochlorothiazide, 0093-3241 — bisoprolol fumarate and hydrochlorothiazide, 0093-3242 — bisoprolol fumarate and hydrochlorothiazide, 0093-3243 — bisoprolol fumarate and hydrochlorothiazide, 0093-5002 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0093-5004 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0093-5005 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0093-5006 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0093-7367 — Losartan Potassium and Hydrochlorothiazide, 0093-7368 — Losartan Potassium and Hydrochlorothiazide, 0093-7369 — Losartan Potassium and Hydrochlorothiazide, 0093-8232 — Irbesartan and Hydrochlorothiazide, 0093-8238 — Irbesartan and Hydrochlorothiazide, 0172-2083 — Hydrochlorothiazide, 0172-2089 — Hydrochlorothiazide, +1450 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.