Irbesartan

NDC 71335-2168 · Bryant Ranch Prepack

Generic nameIrbesartan

Dosage formTABLET

RouteORAL

Active ingredient(s)IRBESARTAN

Strength150 mg/1

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

Marketing categoryANDA

Packages

71335-2168-1 — 30 TABLET in 1 BOTTLE (71335-2168-1)

71335-2168-2 — 60 TABLET in 1 BOTTLE (71335-2168-2)

71335-2168-3 — 90 TABLET in 1 BOTTLE (71335-2168-3)

FDA lists these products with the same active ingredient.

71205-379 — Irbesartan, 71205-452 — Irbesartan, 71335-0071 — Irbesartan, 71335-1097 — Irbesartan and Hydrochlorothiazide, 71335-1244 — Irbesartan, 71335-1263 — Irbesartan, 71335-1547 — Irbesartan, 71335-1787 — Irbesartan and Hydrochlorothiazide, 71335-1826 — Irbesartan, 71335-2099 — Irbesartan and Hydrochlorothiazide, 71335-2745 — Irbesartan, 72162-1035 — Irbesartan and Hydrochlorothiazide, 72162-2317 — Irbesartan and Hydrochlorothiazide, 72162-2354 — Irbesartan, 72162-2355 — Irbesartan, 72189-201 — IRBESARTAN, 72189-205 — IRBESARTAN, 72189-270 — IRBESARTAN, 72205-327 — Irbesartan, 72205-328 — Irbesartan, +95 more

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