NDC 53746-753 – Benazepril Hydrochloride

Benazepril Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC53746-753

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076820
Marketed since
September 26, 2022
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
53746-753-01100 TABLET in 1 BOTTLE (53746-753-01)Sep 26, 2022
53746-753-05500 TABLET in 1 BOTTLE (53746-753-05)Sep 26, 2022

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