Package 44567-245-85

Brand: cefoxitin

Generic: cefoxitin
NDC Package

Package Facts

Identity

Package NDC 44567-245-85
Digits Only 4456724585
Product NDC 44567-245
Product ID 44567-245_f8445b8a-621d-4fd1-a8b6-de87d6f23080
Description

25 VIAL in 1 CARTON (44567-245-85) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2017-07-10
Brand cefoxitin
Generic cefoxitin
Sample Package No

Linked Drug Pages (1)

Cefoxitin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "f8445b8a-621d-4fd1-a8b6-de87d6f23080", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["1665102", "1665107"], "spl_set_id": ["91ac4c14-8dd8-4efe-a462-d1c488a6184f"], "manufacturer_name": ["WG Critical Care, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (44567-245-85)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "44567-245-85", "marketing_start_date": "20170710"}], "brand_name": "Cefoxitin", "product_id": "44567-245_f8445b8a-621d-4fd1-a8b6-de87d6f23080", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "44567-245", "generic_name": "Cefoxitin", "labeler_name": "WG Critical Care, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065414", "marketing_category": "ANDA", "marketing_start_date": "20170710", "listing_expiration_date": "20261231"}