NDC 72189-110 – Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC72189-110

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
DIRECT RX
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA076118
Marketed since
June 12, 2020
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
72189-110-3030 TABLET, COATED in 1 BOTTLE (72189-110-30)Jun 12, 2020
72189-110-9090 TABLET, COATED in 1 BOTTLE (72189-110-90)Jun 12, 2020

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