NDC 68071-1770 – Benazepril Hydrochloride

Benazepril Hydrochloride 40 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC68071-1770

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
NuCare 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 (1)

Package NDCDescriptionSince
68071-1770-1100 TABLET, COATED in 1 BOTTLE (68071-1770-1)Aug 2, 2017

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