NDC 71205-244 – Benazepril Hydrochloride

Benazepril Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-244

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Proficient Rx LP
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 (3)

Package NDCDescriptionSince
71205-244-3030 TABLET in 1 BOTTLE (71205-244-30)Mar 1, 2019
71205-244-6060 TABLET in 1 BOTTLE (71205-244-60)Mar 1, 2019
71205-244-9090 TABLET in 1 BOTTLE (71205-244-90)Mar 1, 2019

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