Package 0404-9834-99
Brand: cefazolin
Generic: cefazolinPackage Facts
Identity
Package NDC
0404-9834-99
Digits Only
0404983499
Product NDC
0404-9834
Description
1 VIAL in 1 BAG (0404-9834-99) / 3 mL 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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "5c5cb92a-87b7-42e7-999c-d09323bfa0c3", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["197d5702-2c20-480e-8246-4d0d21f871be"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9834-99) / 3 mL in 1 VIAL", "package_ndc": "0404-9834-99", "marketing_start_date": "20220109"}], "brand_name": "CEFAZOLIN", "product_id": "0404-9834_5c5cb92a-87b7-42e7-999c-d09323bfa0c3", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0404-9834", "generic_name": "cefazolin", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFAZOLIN", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "330 mg/mL"}], "application_number": "ANDA065047", "marketing_category": "ANDA", "marketing_start_date": "20220109", "listing_expiration_date": "20261231"}