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Irbesartan

NDC 29300-214 · Unichem Pharmaceuticals (USA), Inc.

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

29300-214-05 — 500 TABLET in 1 BOTTLE, PLASTIC (29300-214-05)

29300-214-13 — 30 TABLET in 1 BOTTLE, PLASTIC (29300-214-13)

29300-214-19 — 90 TABLET in 1 BOTTLE, PLASTIC (29300-214-19)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0024-5851 — irbesartan, 0024-5852 — irbesartan, 0024-5855 — irbesartan and hydrochlorothiazide, 0024-5856 — irbesartan and hydrochlorothiazide, 0054-0254 — Irbesartan and Hydrochlorothiazide, 0054-0255 — Irbesartan and Hydrochlorothiazide, 0093-8232 — Irbesartan and Hydrochlorothiazide, 0093-8238 — Irbesartan and Hydrochlorothiazide, 29300-212 — Irbesartan, 29300-213 — Irbesartan, 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, +95 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.