Package 0143-9140-25
Brand: cefazolin
Generic: cefazolinPackage Facts
Identity
Package NDC
0143-9140-25
Digits Only
0143914025
Product NDC
0143-9140
Description
25 VIAL in 1 CARTON (0143-9140-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Marketing
Marketing Status
Brand
cefazolin
Generic
cefazolin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e32063de-96fe-4fb4-9176-5a9d6dc4a722", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665060", "2630753"], "spl_set_id": ["6c7761d3-c154-4802-9876-627cd42913f0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0143-9140-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "0143-9140-25", "marketing_start_date": "20230301"}], "brand_name": "Cefazolin", "product_id": "0143-9140_e32063de-96fe-4fb4-9176-5a9d6dc4a722", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9140", "generic_name": "Cefazolin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "3 g/1"}], "application_number": "NDA216109", "marketing_category": "NDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}