Package 60505-6243-4

Brand: cefazolin

Generic: cefazolin
NDC Package

Package Facts

Identity

Package NDC 60505-6243-4
Digits Only 6050562434
Product NDC 60505-6243
Product ID 60505-6243_90d68812-6ff8-4372-a838-b415162dd40e
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (60505-6243-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (60505-6243-0)

Marketing

Marketing Status
Marketed Since 2022-09-01
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "90d68812-6ff8-4372-a838-b415162dd40e", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["37a626aa-96dc-4c4d-bfbc-be4f328f918b"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (60505-6243-4)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (60505-6243-0)", "package_ndc": "60505-6243-4", "marketing_start_date": "20220901"}], "brand_name": "Cefazolin", "product_id": "60505-6243_90d68812-6ff8-4372-a838-b415162dd40e", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "60505-6243", "generic_name": "Cefazolin", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA203661", "marketing_category": "ANDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}