NDC 72162-2317 – Irbesartan and Hydrochlorothiazide

Irbesartan 150 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-2317

Product details

Brand name
Irbesartan and Hydrochlorothiazide
Generic name
Irbesartan and Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203072
Marketed since
March 1, 2014
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 (2)

Package NDCDescriptionSince
72162-2317-330 TABLET in 1 BOTTLE (72162-2317-3)Mar 1, 2014
72162-2317-990 TABLET in 1 BOTTLE (72162-2317-9)Mar 1, 2014

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