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Irbesartan

NDC 71205-379 · Proficient Rx LP

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

71205-379-30 — 30 TABLET in 1 BOTTLE (71205-379-30)

71205-379-60 — 60 TABLET in 1 BOTTLE (71205-379-60)

71205-379-90 — 90 TABLET in 1 BOTTLE (71205-379-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 71205-082 — 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, 71335-2168 — Irbesartan, +95 more

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