Package 84549-142-05

Brand: cefazolin

Generic: cefazolin
NDC Package

Package Facts

Identity

Package NDC 84549-142-05
Digits Only 8454914205
Product NDC 84549-142
Product ID 84549-142_3d5cc73c-8a42-b285-e063-6294a90a609f
Description

1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (84549-142-05)

Marketing

Marketing Status
Marketed Since 2025-09-01
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": "3d5cc73c-8a42-b285-e063-6294a90a609f", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["3d5cc73c-8a41-b285-e063-6294a90a609f"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (84549-142-05)", "package_ndc": "84549-142-05", "marketing_start_date": "20250901"}], "brand_name": "Cefazolin", "product_id": "84549-142_3d5cc73c-8a42-b285-e063-6294a90a609f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "84549-142", "generic_name": "Cefazolin", "labeler_name": "ProPharma Distribution", "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": "20170630", "listing_expiration_date": "20261231"}