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Irbesartan and Hydrochlorothiazide

NDC 65862-631 · Aurobindo Pharma Limited

Generic nameIrbesartan and Hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IRBESARTAN, HYDROCHLOROTHIAZIDE
Strength25; 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

65862-631-05 — 500 TABLET, FILM COATED in 1 BOTTLE (65862-631-05)

65862-631-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-631-30)

65862-631-90 — 90 TABLET, FILM COATED in 1 BOTTLE (65862-631-90)

65862-631-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (65862-631-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-468 — Losartan Potassium and Hydrochlorothiazide, 65862-469 — Losartan Potassium and Hydrochlorothiazide, 65862-470 — Losartan Potassium and Hydrochlorothiazide, 65862-547 — Valsartan and Hydrochlorothiazide, 65862-548 — Valsartan and Hydrochlorothiazide, 65862-549 — Valsartan and Hydrochlorothiazide, 65862-550 — Valsartan and Hydrochlorothiazide, 65862-551 — Valsartan and Hydrochlorothiazide, 65862-629 — Irbesartan and Hydrochlorothiazide, 65862-630 — Irbesartan and Hydrochlorothiazide, 65862-637 — Irbesartan, 65862-638 — Irbesartan, 65862-639 — Irbesartan, 65862-779 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-780 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-781 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-834 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-835 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-836 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-837 — Amlodipine, Valsartan and 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.