Package 0143-9665-10

Brand: cefazolin

Generic: cefazolin
NDC Package

Package Facts

Identity

Package NDC 0143-9665-10
Digits Only 0143966510
Product NDC 0143-9665
Product ID 0143-9665_a1fc6bdd-6f1b-402f-9e84-b6e5ed5febb4
Description

1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9665-10)

Marketing

Marketing Status
Marketed Since 2004-10-18
Brand cefazolin
Generic cefazolin
Sample Package No

Linked Drug Pages (1)

Cefazolin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "a1fc6bdd-6f1b-402f-9e84-b6e5ed5febb4", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["313920"], "spl_set_id": ["06091653-e568-4e82-acc7-aefbce16de17"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9665-10)", "package_ndc": "0143-9665-10", "marketing_start_date": "20041018"}], "brand_name": "Cefazolin", "product_id": "0143-9665_a1fc6bdd-6f1b-402f-9e84-b6e5ed5febb4", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9665", "generic_name": "Cefazolin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "20 g/1"}], "application_number": "ANDA065143", "marketing_category": "ANDA", "marketing_start_date": "20041018", "listing_expiration_date": "20261231"}