NDC 70518-4633 – Benazepril Hydrochloride

Benazepril Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-4633

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076267
Marketed since
April 25, 2026
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 (1)

Package NDCDescriptionSince
70518-4633-090 TABLET in 1 BOTTLE, PLASTIC (70518-4633-0)Apr 25, 2026

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