NDC 71335-0854 – Benazepril Hydrochloride

Benazepril Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0854

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076820
Marketed since
February 2, 2010
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
71335-0854-130 TABLET in 1 BOTTLE (71335-0854-1)Aug 17, 2018
71335-0854-260 TABLET in 1 BOTTLE (71335-0854-2)Mar 9, 2022
71335-0854-3100 TABLET in 1 BOTTLE (71335-0854-3)Apr 11, 2022
71335-0854-490 TABLET in 1 BOTTLE (71335-0854-4)Jun 11, 2018

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