NDC 50090-3775 – Benazepril Hydrochloride

Benazepril Hydrochloride 10 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC50090-3775

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
A-S Medication Solutions
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
50090-3775-030 TABLET, COATED in 1 BOTTLE (50090-3775-0)Nov 5, 2018
50090-3775-290 TABLET, COATED in 1 BOTTLE (50090-3775-2)Nov 5, 2018

Other Benazepril Hydrochloride products