Package 52652-5001-1

Brand: katerzia

Generic: amlodipine
NDC Package

Package Facts

Identity

Package NDC 52652-5001-1
Digits Only 5265250011
Product NDC 52652-5001
Description

1 BOTTLE in 1 CARTON (52652-5001-1) / 150 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-08-15
Brand katerzia
Generic amlodipine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "461e8d10-1805-e107-e063-6294a90aa288", "openfda": {"unii": ["XD75TQ8A2P"], "rxcui": ["2184120", "2184126"], "spl_set_id": ["df673a4d-acb8-444c-a472-c87ab8cbd366"], "manufacturer_name": ["Azurity Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (52652-5001-1)  / 150 mL in 1 BOTTLE", "package_ndc": "52652-5001-1", "marketing_start_date": "20190815"}], "brand_name": "Katerzia", "product_id": "52652-5001_461e8d10-1805-e107-e063-6294a90aa288", "dosage_form": "SUSPENSION", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "52652-5001", "generic_name": "Amlodipine", "labeler_name": "Azurity Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Katerzia", "active_ingredients": [{"name": "AMLODIPINE BENZOATE", "strength": "1 mg/mL"}], "application_number": "NDA211340", "marketing_category": "NDA", "marketing_start_date": "20190815", "listing_expiration_date": "20261231"}