NDC 65162-752 – Benazepril Hydrochloride

Benazepril Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC65162-752

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Amneal Pharmaceuticals LLC
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
65162-752-0330 TABLET in 1 BOTTLE (65162-752-03)Feb 2, 2010
65162-752-10100 TABLET in 1 BOTTLE (65162-752-10)Feb 2, 2010
65162-752-50500 TABLET in 1 BOTTLE (65162-752-50)Feb 2, 2010

Recalls mentioning this NDC

Other Benazepril Hydrochloride products