NDC 51655-066 – Benazepril Hydrochloride

Benazepril Hydrochloride 20 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC51655-066

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA076118
Marketed since
March 4, 2016
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Benazepril Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
51655-066-2690 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-066-26)Jul 11, 2022
51655-066-5230 TABLET, COATED in 1 BOTTLE, DISPENSING (51655-066-52)Mar 4, 2016

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