NDC 68788-6889 – Benazepril Hydrochloride

Benazepril Hydrochloride 5 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC68788-6889

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA076118
Marketed since
February 6, 2017
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 (5)

Package NDCDescriptionSince
68788-6889-1100 TABLET, COATED in 1 BOTTLE (68788-6889-1)Feb 6, 2017
68788-6889-330 TABLET, COATED in 1 BOTTLE (68788-6889-3)Feb 6, 2017
68788-6889-660 TABLET, COATED in 1 BOTTLE (68788-6889-6)Feb 6, 2017
68788-6889-8120 TABLET, COATED in 1 BOTTLE (68788-6889-8)Feb 6, 2017
68788-6889-990 TABLET, COATED in 1 BOTTLE (68788-6889-9)Feb 6, 2017

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