NDC 68071-1969 – Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC68071-1969

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 (4)

Package NDCDescriptionSince
68071-1969-2120 TABLET, COATED in 1 BOTTLE (68071-1969-2)Jul 2, 2018
68071-1969-330 TABLET, COATED in 1 BOTTLE (68071-1969-3)Jul 2, 2018
68071-1969-660 TABLET, COATED in 1 BOTTLE (68071-1969-6)Jul 2, 2018
68071-1969-990 TABLET, COATED in 1 BOTTLE (68071-1969-9)Jul 2, 2018

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