NDC 43547-338 – Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC43547-338

Product details

Brand name
Benazepril Hydrochloride
Generic name
Benazepril Hydrochloride
Labeler
Solco healthcare U.S., LLC
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 (3)

Package NDCDescriptionSince
43547-338-0330 TABLET, COATED in 1 BOTTLE (43547-338-03)Jun 30, 2019
43547-338-10100 TABLET, COATED in 1 BOTTLE (43547-338-10)Jan 1, 2014
43547-338-50500 TABLET, COATED in 1 BOTTLE (43547-338-50)Jan 1, 2014

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