NDC 51655-213 – Amlodipine and Benazepril Hydrochloride

Amlodipine Besylate 10 mg/1; Benazepril Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC51655-213

Product details

Brand name
Amlodipine and Benazepril Hydrochloride
Generic name
Amlodipine and Benazepril Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA202239
Marketed since
October 20, 2022
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 (2)

Package NDCDescriptionSince
51655-213-2690 CAPSULE in 1 BOTTLE, PLASTIC (51655-213-26)Oct 20, 2022
51655-213-5230 CAPSULE in 1 BOTTLE, PLASTIC (51655-213-52)May 2, 2023

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