NDC 63187-500 – Benazepril Hydrochloride

Benazepril Hydrochloride 5 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC63187-500

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA076118
Marketed since
January 1, 2014
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 (3)

Package NDCDescriptionSince
63187-500-3030 TABLET, COATED in 1 BOTTLE (63187-500-30)Feb 2, 2015
63187-500-6060 TABLET, COATED in 1 BOTTLE (63187-500-60)Feb 2, 2015
63187-500-9090 TABLET, COATED in 1 BOTTLE (63187-500-90)Feb 2, 2015

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