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IRBESARTAN

NDC 62135-976 · Chartwell RX, LLC

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

62135-976-30 — 30 TABLET in 1 BOTTLE (62135-976-30)

62135-976-90 — 90 TABLET in 1 BOTTLE (62135-976-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6938 — Irbesartan, 50090-7622 — Irbesartan, 50228-160 — Irbesartan, 50228-161 — Irbesartan, 50228-162 — Irbesartan, 50268-441 — Irbesartan, 50268-442 — Irbesartan, 59746-447 — IRBESARTAN, 59746-448 — IRBESARTAN, 59746-449 — IRBESARTAN, 62135-977 — IRBESARTAN, 62135-978 — IRBESARTAN, 62332-041 — IRBESARTAN, 62332-042 — IRBESARTAN, 62332-043 — IRBESARTAN, 62332-051 — Irbesartan and Hydrochlorothiazide, 62332-052 — Irbesartan and Hydrochlorothiazide, 62332-053 — Irbesartan and Hydrochlorothiazide, 63187-653 — Irbesartan and Hydrochlorothiazide, 63187-737 — 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.