Package 0264-3125-11

Brand: cefoxitin and dextrose

Generic: cefoxitin sodium
NDC Package

Package Facts

Identity

Package NDC 0264-3125-11
Digits Only 0264312511
Product NDC 0264-3125
Description

24 CONTAINER in 1 CASE (0264-3125-11) / 50 mL in 1 CONTAINER

Marketing

Marketing Status
Marketed Since 2006-03-10
Brand cefoxitin and dextrose
Generic cefoxitin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0cca0e6a-3047-4142-af33-d9b98efe85b1", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["1665102", "1665107"], "spl_set_id": ["6c7e9485-1ede-411c-8c46-911439332864"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 CONTAINER in 1 CASE (0264-3125-11)  / 50 mL in 1 CONTAINER", "package_ndc": "0264-3125-11", "marketing_start_date": "20060310"}], "brand_name": "Cefoxitin and Dextrose", "product_id": "0264-3125_0cca0e6a-3047-4142-af33-d9b98efe85b1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0264-3125", "generic_name": "CEFOXITIN SODIUM", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin and Dextrose", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "2 g/50mL"}], "application_number": "NDA065214", "marketing_category": "NDA", "marketing_start_date": "20060310", "listing_expiration_date": "20261231"}