Package 72189-584-01

Brand: cefazolin sodium

Generic: cefazolin sodium
NDC Package

Package Facts

Identity

Package NDC 72189-584-01
Digits Only 7218958401
Product NDC 72189-584
Product ID 72189-584_22dfc2e4-07a8-8d13-e063-6394a90a3e9f
Description

1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (72189-584-01)

Marketing

Marketing Status
Marketed Since 2024-09-24
Brand cefazolin sodium
Generic cefazolin sodium
Sample Package No

Linked Drug Pages (1)

Cefazolin Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "22dfc2e4-07a8-8d13-e063-6394a90a3e9f", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["22dfc2e4-07a7-8d13-e063-6394a90a3e9f"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (72189-584-01)", "package_ndc": "72189-584-01", "marketing_start_date": "20240924"}], "brand_name": "Cefazolin Sodium", "product_id": "72189-584_22dfc2e4-07a8-8d13-e063-6394a90a3e9f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "72189-584", "generic_name": "Cefazolin Sodium", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin Sodium", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA203661", "marketing_category": "ANDA", "marketing_start_date": "20240924", "listing_expiration_date": "20261231"}