Package 0143-9876-10

Brand: cefoxitin

Generic: cefoxitin
NDC Package

Package Facts

Identity

Package NDC 0143-9876-10
Digits Only 0143987610
Product NDC 0143-9876
Product ID 0143-9876_3de36693-e566-4f2a-b9fe-8b777b275fa4
Description

10 BOTTLE in 1 CARTON (0143-9876-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE (0143-9876-01)

Marketing

Marketing Status
Marketed Since 2010-02-26
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": "3de36693-e566-4f2a-b9fe-8b777b275fa4", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["309072"], "spl_set_id": ["6a4a2afa-4f00-41d4-bd6d-baa0a95f6929"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BOTTLE in 1 CARTON (0143-9876-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE (0143-9876-01)", "package_ndc": "0143-9876-10", "marketing_start_date": "20100226"}], "brand_name": "Cefoxitin", "product_id": "0143-9876_3de36693-e566-4f2a-b9fe-8b777b275fa4", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9876", "generic_name": "Cefoxitin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "10 g/1"}], "application_number": "ANDA065239", "marketing_category": "ANDA", "marketing_start_date": "20100226", "listing_expiration_date": "20261231"}