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Irbesartan

NDC 63629-8259 · Bryant Ranch Prepack

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

63629-8259-1 — 30 TABLET in 1 BOTTLE (63629-8259-1)

63629-8259-2 — 90 TABLET in 1 BOTTLE (63629-8259-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 63187-981 — Irbesartan and Hydrochlorothiazide, 63629-5241 — Irbesartan, 63629-7468 — Irbesartan and Hydrochlorothiazide, 65162-284 — Irbesartan, 65162-285 — Irbesartan, 65162-286 — Irbesartan, 65862-629 — Irbesartan and Hydrochlorothiazide, 65862-630 — Irbesartan and Hydrochlorothiazide, 65862-631 — Irbesartan and Hydrochlorothiazide, 65862-637 — Irbesartan, 65862-638 — Irbesartan, 65862-639 — Irbesartan, 68180-411 — 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.