Package 25021-109-10

Brand: cefoxitin

Generic: cefoxitin
NDC Package

Package Facts

Identity

Package NDC 25021-109-10
Digits Only 2502110910
Product NDC 25021-109
Product ID 25021-109_b43cf6e8-a0e4-4f66-9559-6fcc65c40532
Description

10 VIAL in 1 CARTON (25021-109-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2009-11-05
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": "b43cf6e8-a0e4-4f66-9559-6fcc65c40532", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["1665102", "1665107"], "spl_set_id": ["b272ef9c-4d83-4ee2-b9cc-477440822cca"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-109-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "25021-109-10", "marketing_start_date": "20091105"}], "brand_name": "Cefoxitin", "product_id": "25021-109_b43cf6e8-a0e4-4f66-9559-6fcc65c40532", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "25021-109", "generic_name": "cefoxitin", "labeler_name": "Sagent Pharmaceuticals", "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": "20091105", "listing_expiration_date": "20261231"}