NDC 63187-393 – Benazepril Hydrochloride

Benazepril Hydrochloride 20 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC63187-393

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 (2)

Package NDCDescriptionSince
63187-393-3030 TABLET, COATED in 1 BOTTLE (63187-393-30)Sep 1, 2016
63187-393-9090 TABLET, COATED in 1 BOTTLE (63187-393-90)Sep 1, 2016

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