NDC 43063-677 – Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC43063-677

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
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
43063-677-3030 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-677-30)Jun 9, 2016
43063-677-9090 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-677-90)Jun 7, 2024

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