NDC 51655-755 – Benazepril Hydrochloride

Benazepril Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-755

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076820
Marketed since
April 3, 2023
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
51655-755-2690 TABLET in 1 BOTTLE, PLASTIC (51655-755-26)Nov 14, 2023
51655-755-5230 TABLET in 1 BOTTLE, PLASTIC (51655-755-52)Apr 3, 2023

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