NDC 51655-201 – Amlodipine Besylate and Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC51655-201

Product details

Brand name
Amlodipine Besylate and Benazepril Hydrochloride
Generic name
Amlodipine Besylate and Benazepril Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077183
Marketed since
April 19, 2023
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 Besylate and Benazepril Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
51655-201-5230 CAPSULE in 1 BOTTLE, PLASTIC (51655-201-52)Apr 19, 2023

Other Amlodipine Besylate and Benazepril Hydrochloride products