NDC 71335-1086 – Benazepril Hydrochloride

Benazepril Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1086

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 (6)

Package NDCDescriptionSince
71335-1086-130 TABLET in 1 BOTTLE (71335-1086-1)May 4, 2022
71335-1086-260 TABLET in 1 BOTTLE (71335-1086-2)May 4, 2022
71335-1086-3100 TABLET in 1 BOTTLE (71335-1086-3)May 4, 2022
71335-1086-490 TABLET in 1 BOTTLE (71335-1086-4)May 4, 2022
71335-1086-514 TABLET in 1 BOTTLE (71335-1086-5)May 4, 2022
71335-1086-610 TABLET in 1 BOTTLE (71335-1086-6)May 4, 2022

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