Package 0338-0096-06

Brand: cefazolin

Generic: cefazolin sodium
NDC Package

Package Facts

Identity

Package NDC 0338-0096-06
Digits Only 0338009606
Product NDC 0338-0096
Description

6 BAG in 1 CARTON (0338-0096-06) / 150 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2024-05-31
Brand cefazolin
Generic cefazolin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b0e63b97-7941-485b-bd92-98cbd0fc1b71", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050", "1665060", "2630753"], "spl_set_id": ["d91a8d13-99a0-4d87-88dc-71cbd37922b4"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BAG in 1 CARTON (0338-0096-06)  / 150 mL in 1 BAG", "package_ndc": "0338-0096-06", "marketing_start_date": "20240531"}], "brand_name": "Cefazolin", "product_id": "0338-0096_b0e63b97-7941-485b-bd92-98cbd0fc1b71", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0338-0096", "generic_name": "Cefazolin Sodium", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "3 g/150mL"}], "application_number": "NDA207131", "marketing_category": "NDA", "marketing_start_date": "20240531", "listing_expiration_date": "20261231"}