NDC 69238-2687 – Amlodipine Besylate and Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC69238-2687

Product details

Brand name
Amlodipine Besylate and Benazepril Hydrochloride
Generic name
Amlodipine Besylate and Benazepril Hydrochloride
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077215
Marketed since
April 14, 2026
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
69238-2687-1100 CAPSULE in 1 BOTTLE (69238-2687-1)Apr 14, 2026

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