Irbesartan

NDC 65862-639 · Aurobindo Pharma Limited

Generic nameIrbesartan

Dosage formTABLET

RouteORAL

Active ingredient(s)IRBESARTAN

Strength300 mg/1

Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]

Marketing categoryANDA

Packages

65862-639-05 — 500 TABLET in 1 BOTTLE (65862-639-05)

65862-639-30 — 30 TABLET in 1 BOTTLE (65862-639-30)

65862-639-78 — 10 BLISTER PACK in 1 CARTON (65862-639-78) / 10 TABLET in 1 BLISTER PACK (65862-639-10)

65862-639-90 — 90 TABLET in 1 BOTTLE (65862-639-90)

FDA lists these products with the same active ingredient.

63629-7468 — Irbesartan and Hydrochlorothiazide, 63629-8259 — Irbesartan, 65162-284 — Irbesartan, 65162-285 — Irbesartan, 65162-286 — Irbesartan, 65862-629 — Irbesartan and Hydrochlorothiazide, 65862-630 — Irbesartan and Hydrochlorothiazide, 65862-631 — Irbesartan and Hydrochlorothiazide, 65862-637 — Irbesartan, 65862-638 — Irbesartan, 68180-411 — Irbesartan, 68180-412 — Irbesartan, 68788-8670 — Irbesartan, 70518-1543 — Irbesartan, 70518-1550 — Irbesartan and Hydrochlorothiazide, 70518-1690 — Irbesartan, 70518-2245 — Irbesartan, 70518-2246 — Irbesartan, 70518-2685 — Irbesartan, 71205-063 — Irbesartan and Hydrochlorothiazide, +95 more

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