NDC 50268-109 – Benazepril Hydrochloride

Benazepril Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50268-109

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
AvPAK
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076820
Marketed since
April 28, 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
50268-109-1550 BLISTER PACK in 1 BOX (50268-109-15) / 1 TABLET in 1 BLISTER PACK (50268-109-11)Apr 28, 2014

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