NDC 50090-6185 – Amlodipine Besylate and Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC50090-6185

Product details

Brand name
Amlodipine Besylate and Benazepril Hydrochloride
Generic name
Amlodipine Besylate and Benazepril Hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078466
Marketed since
August 1, 2018
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 (2)

Package NDCDescriptionSince
50090-6185-030 CAPSULE in 1 BOTTLE (50090-6185-0)Oct 25, 2022
50090-6185-190 CAPSULE in 1 BOTTLE (50090-6185-1)Oct 25, 2022

Other Amlodipine Besylate and Benazepril Hydrochloride products