NDC 63187-906 – Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC63187-906

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
63187-906-3030 TABLET, COATED in 1 BOTTLE (63187-906-30)Sep 1, 2017
63187-906-6060 TABLET, COATED in 1 BOTTLE (63187-906-60)Sep 1, 2017
63187-906-9090 TABLET, COATED in 1 BOTTLE (63187-906-90)Sep 1, 2017

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