NDC 23155-923 – Amlodipine and Benazepril Hydrochloride

Amlodipine Besylate 5 mg/1; Benazepril Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC23155-923

Product details

Brand name
Amlodipine and Benazepril Hydrochloride
Generic name
Amlodipine and Benazepril Hydrochloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA091431
Marketed since
July 24, 2026
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Amlodipine and Benazepril Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
23155-923-01100 CAPSULE in 1 BOTTLE (23155-923-01)Jul 24, 2026
23155-923-05500 CAPSULE in 1 BOTTLE (23155-923-05)Jul 24, 2026
23155-923-101000 CAPSULE in 1 BOTTLE (23155-923-10)Jul 24, 2026

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