Package 0143-9923-90

Brand: cefazolin

Generic: cefazolin
NDC Package

Package Facts

Identity

Package NDC 0143-9923-90
Digits Only 0143992390
Product NDC 0143-9923
Product ID 0143-9923_a4e97132-f711-404f-93b8-8ee5e4254c96
Description

2.2 mL in 1 VIAL (0143-9923-90)

Marketing

Marketing Status
Marketed Since 2001-09-18
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "a4e97132-f711-404f-93b8-8ee5e4254c96", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050", "1665052"], "spl_set_id": ["1dc9de56-e259-4546-a1db-23119a8a088e"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2.2 mL in 1 VIAL (0143-9923-90)", "package_ndc": "0143-9923-90", "marketing_start_date": "20010918"}], "brand_name": "Cefazolin", "product_id": "0143-9923_a4e97132-f711-404f-93b8-8ee5e4254c96", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9923", "generic_name": "Cefazolin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "225 mg/mL"}], "application_number": "ANDA065047", "marketing_category": "ANDA", "marketing_start_date": "20010918", "listing_expiration_date": "20261231"}