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Irbesartan

NDC 70518-1690 · REMEDYREPACK INC.

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

70518-1690-1 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-1690-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-630 — Irbesartan and Hydrochlorothiazide, 65862-631 — Irbesartan and Hydrochlorothiazide, 65862-637 — Irbesartan, 65862-638 — Irbesartan, 65862-639 — Irbesartan, 68180-411 — Irbesartan, 68180-412 — Irbesartan, 68788-8670 — Irbesartan, 70518-1543 — Irbesartan, 70518-1550 — Irbesartan and Hydrochlorothiazide, 70518-2245 — Irbesartan, 70518-2246 — Irbesartan, 70518-2685 — 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, +95 more

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