NDC 68788-8454 – Amlodipine and Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC68788-8454

Product details

Brand name
Amlodipine and Benazepril Hydrochloride
Generic name
Amlodipine and Benazepril Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA202239
Marketed since
June 2, 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 and Benazepril Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
68788-8454-330 CAPSULE in 1 BOTTLE (68788-8454-3)Jun 2, 2023

Other Amlodipine and Benazepril Hydrochloride products