NDC 68788-8877 – Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC68788-8877

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078212
Marketed since
May 19, 2025
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 (4)

Package NDCDescriptionSince
68788-8877-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8877-1)May 19, 2025
68788-8877-330 TABLET, FILM COATED in 1 BOTTLE (68788-8877-3)May 19, 2025
68788-8877-660 TABLET, FILM COATED in 1 BOTTLE (68788-8877-6)May 19, 2025
68788-8877-990 TABLET, FILM COATED in 1 BOTTLE (68788-8877-9)May 19, 2025

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