NDC 52652-5001 – Katerzia

Amlodipine Benzoate 1 mg/mL · Suspension · Oral

Human Prescription Drug

Product NDC52652-5001

Product details

Brand name
Katerzia
Generic name
Amlodipine
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
Suspension
Route
Oral
Marketing category
NDA · NDA211340
Marketed since
August 15, 2019
Listing expires
December 31, 2026
Pharmacologic class
Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Katerzia →

Package NDC codes (1)

Package NDCDescriptionSince
52652-5001-11 BOTTLE in 1 CARTON (52652-5001-1) / 150 mL in 1 BOTTLEAug 15, 2019