Package 0143-9878-25

Brand: cefoxitin

Generic: cefoxitin
NDC Package

Package Facts

Identity

Package NDC 0143-9878-25
Digits Only 0143987825
Product NDC 0143-9878
Product ID 0143-9878_4638263b-1c03-4a32-ba82-70270cf42490
Description

25 VIAL in 1 CARTON (0143-9878-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01)

Marketing

Marketing Status
Marketed Since 2010-03-12
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": "4638263b-1c03-4a32-ba82-70270cf42490", "openfda": {"unii": ["Q68050H03T"], "rxcui": ["1665102", "1665107"], "spl_set_id": ["d2c449b9-5624-4166-95b1-d7813b3d0445"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0143-9878-25)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01)", "package_ndc": "0143-9878-25", "marketing_start_date": "20100312"}], "brand_name": "Cefoxitin", "product_id": "0143-9878_4638263b-1c03-4a32-ba82-70270cf42490", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9878", "generic_name": "Cefoxitin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065238", "marketing_category": "ANDA", "marketing_start_date": "20100312", "listing_expiration_date": "20261231"}