NDC 71205-320 – Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC71205-320

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078212
Marketed since
May 22, 2008
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
71205-320-3030 TABLET, FILM COATED in 1 BOTTLE (71205-320-30)Sep 1, 2019
71205-320-6060 TABLET, FILM COATED in 1 BOTTLE (71205-320-60)Sep 1, 2019
71205-320-9090 TABLET, FILM COATED in 1 BOTTLE (71205-320-90)Sep 1, 2019

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