Package 25021-111-99

Brand: cefoxitin

Generic: cefoxitin
NDC Package

Package Facts

Identity

Package NDC 25021-111-99
Digits Only 2502111199
Product NDC 25021-111
Product ID 25021-111_79813968-4f6f-49a9-9a94-18607a1bcfbf
Description

10 BOTTLE in 1 CARTON (25021-111-99) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2010-08-12
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": "79813968-4f6f-49a9-9a94-18607a1bcfbf", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["309072"], "spl_set_id": ["4c6f7665-204f-6c69-7669-61204d756e6e"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BOTTLE in 1 CARTON (25021-111-99)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE", "package_ndc": "25021-111-99", "marketing_start_date": "20100812"}], "brand_name": "Cefoxitin", "product_id": "25021-111_79813968-4f6f-49a9-9a94-18607a1bcfbf", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "25021-111", "generic_name": "cefoxitin", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "10 g/1"}], "application_number": "ANDA065415", "marketing_category": "ANDA", "marketing_start_date": "20100812", "listing_expiration_date": "20261231"}