NDC 72162-1035 – Irbesartan and Hydrochlorothiazide

Irbesartan 150 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72162-1035

Product details

Brand name
Irbesartan and Hydrochlorothiazide
Generic name
Irbesartan and Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077369
Marketed since
January 24, 2013
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Irbesartan and Hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
72162-1035-990 TABLET, FILM COATED in 1 BOTTLE (72162-1035-9)Apr 7, 2026

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