NDC 71335-1365 – Benazepril Hydrochloride

Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1365

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078212
Marketed since
May 22, 2008
Marketing end
November 30, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Benazepril Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
71335-1365-130 TABLET, FILM COATED in 1 BOTTLE (71335-1365-1)Feb 13, 2020
71335-1365-2100 TABLET, FILM COATED in 1 BOTTLE (71335-1365-2)Oct 7, 2019
71335-1365-360 TABLET, FILM COATED in 1 BOTTLE (71335-1365-3)May 30, 2024
71335-1365-490 TABLET, FILM COATED in 1 BOTTLE (71335-1365-4)Mar 11, 2020

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