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Irbesartan and Hydrochlorothiazide

NDC 0093-8232 · Teva Pharmaceuticals USA, Inc.

Generic nameIrbesartan and Hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IRBESARTAN, HYDROCHLOROTHIAZIDE
Strength12.5; 300 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

0093-8232-56 — 30 TABLET, FILM COATED in 1 BOTTLE (0093-8232-56)

0093-8232-98 — 90 TABLET, FILM COATED in 1 BOTTLE (0093-8232-98)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-3242 — bisoprolol fumarate and hydrochlorothiazide, 0093-3243 — bisoprolol fumarate and hydrochlorothiazide, 0093-5002 — Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide, 0093-5003 — 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, 0093-8238 — Irbesartan and Hydrochlorothiazide, 0172-2083 — Hydrochlorothiazide, 0172-2089 — Hydrochlorothiazide, 0172-3444 — Hydrochlorothiazide, 0185-0211 — Benazepril Hydrochloride and Hydrochlorothiazide, 0185-0236 — Benazepril Hydrochloride and Hydrochlorothiazide, 0185-0277 — Benazepril Hydrochloride and Hydrochlorothiazide, 0185-0325 — Benazepril Hydrochloride and Hydrochlorothiazide, 0187-0146 — enalapril maleate and hydrochlorothiazide, 0228-2820 — Hydrochlorothiazide, +940 more

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