NDC 71205-122 – Amlodipine and Benazepril Hydrochloride

Amlodipine Besylate 5 mg/1; Benazepril Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71205-122

Product details

Brand name
Amlodipine and Benazepril Hydrochloride
Generic name
Amlodipine and Benazepril Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA202239
Marketed since
September 5, 2012
Listing expires
December 31, 2026
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
71205-122-3030 CAPSULE in 1 BOTTLE (71205-122-30)Sep 4, 2018
71205-122-6060 CAPSULE in 1 BOTTLE (71205-122-60)Sep 4, 2018
71205-122-9090 CAPSULE in 1 BOTTLE (71205-122-90)Sep 4, 2018

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