NDC 72162-2328 – Benazepril hydrochloride and hydrochlorothiazide

Benazepril Hydrochloride 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-2328

Product details

Brand name
Benazepril hydrochloride and hydrochlorothiazide
Generic name
Benazepril hydrochloride and hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA020033
Marketed since
April 7, 2019
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Benazepril hydrochloride and hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
72162-2328-1100 TABLET in 1 BOTTLE (72162-2328-1)Jun 18, 2024

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