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Irbesartan

NDC 33342-049 · Macleods 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

33342-049-07 — 30 TABLET in 1 BOTTLE (33342-049-07)

33342-049-10 — 90 TABLET in 1 BOTTLE (33342-049-10)

33342-049-15 — 500 TABLET in 1 BOTTLE (33342-049-15)

33342-049-39 — 9 BLISTER PACK in 1 CARTON (33342-049-39) / 10 TABLET in 1 BLISTER PACK

33342-049-76 — 3400 TABLET in 1 POUCH (33342-049-76)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

29300-215 — Irbesartan and Hydrochlorothiazide, 29300-216 — Irbesartan and Hydrochlorothiazide, 31722-160 — Irbesartan, 31722-161 — Irbesartan, 31722-162 — Irbesartan, 31722-729 — Irbesartan, 31722-730 — Irbesartan, 31722-731 — Irbesartan, 33342-047 — Irbesartan, 33342-048 — Irbesartan, 33342-057 — Irbesartan and Hydrochlorothiazide, 33342-058 — Irbesartan and Hydrochlorothiazide, 42291-940 — IRBESARTAN, 42291-941 — IRBESARTAN, 42291-942 — IRBESARTAN, 42658-121 — IRBESARTAN, 42658-122 — IRBESARTAN, 42658-123 — IRBESARTAN, 43547-330 — Irbesartan and Hydrochlorothiazide, 43547-331 — Irbesartan and Hydrochlorothiazide, +95 more

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