NDC 70518-4386 – Amlodipine Besylate and Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC70518-4386

Product details

Brand name
Amlodipine Besylate and Benazepril Hydrochloride
Generic name
Amlodipine Besylate and Benazepril Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078466
Marketed since
July 6, 2025
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
70518-4386-090 CAPSULE in 1 BOTTLE, PLASTIC (70518-4386-0)Jul 6, 2025

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