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IRBESARTAN

NDC 46708-441 · Alembic Pharmaceuticals Limited

Generic nameIRBESARTAN
Dosage formTABLET
RouteORAL
Active ingredient(s)IRBESARTAN
Strength300 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

46708-441-30 — 30 TABLET in 1 BOTTLE (46708-441-30)

46708-441-31 — 100 TABLET in 1 BOTTLE (46708-441-31)

46708-441-71 — 500 TABLET in 1 BOTTLE (46708-441-71)

46708-441-90 — 90 TABLET in 1 BOTTLE (46708-441-90)

46708-441-91 — 1000 TABLET in 1 BOTTLE (46708-441-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42658-121 — IRBESARTAN, 42658-122 — IRBESARTAN, 42658-123 — IRBESARTAN, 43547-330 — Irbesartan and Hydrochlorothiazide, 43547-331 — Irbesartan and Hydrochlorothiazide, 43547-374 — Irbesartan, 43547-375 — Irbesartan, 43547-376 — Irbesartan, 46708-439 — IRBESARTAN, 46708-440 — IRBESARTAN, 46708-442 — Irbesartan and Hydrochlorothiazide, 46708-443 — Irbesartan and Hydrochlorothiazide, 46708-444 — Irbesartan and Hydrochlorothiazide, 50090-1284 — Irbesartan, 50090-2017 — Irbesartan, 50090-2978 — Irbesartan, 50090-6938 — Irbesartan, 50090-7622 — Irbesartan, 50228-160 — Irbesartan, 50228-161 — 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.