NDC 71335-1946 – Amlodipine Besylate and Benazepril Hydrochloride

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

Human Prescription Drug

Product NDC71335-1946

Product details

Brand name
Amlodipine Besylate and Benazepril Hydrochloride
Generic name
Amlodipine Besylate and Benazepril Hydrochloride
Labeler
Bryant Ranch Prepack
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 (4)

Package NDCDescriptionSince
71335-1946-130 CAPSULE in 1 BOTTLE (71335-1946-1)Sep 21, 2021
71335-1946-290 CAPSULE in 1 BOTTLE (71335-1946-2)Sep 21, 2021
71335-1946-360 CAPSULE in 1 BOTTLE (71335-1946-3)Sep 21, 2021
71335-1946-4100 CAPSULE in 1 BOTTLE (71335-1946-4)Sep 21, 2021

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