Irbesartan

NDC 70518-2685 · REMEDYREPACK INC.

Generic nameIrbesartan

Dosage formTABLET

RouteORAL

Active ingredient(s)IRBESARTAN

Strength75 mg/1

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

Marketing categoryANDA

Packages

70518-2685-0 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-2685-0)

FDA lists these products with the same active ingredient.

65862-638 — Irbesartan, 65862-639 — 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, 71205-063 — Irbesartan and Hydrochlorothiazide, 71205-082 — Irbesartan, 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, +95 more

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