Package 0143-9671-10

Brand: cefotetan

Generic: cefotetan
NDC Package

Package Facts

Identity

Package NDC 0143-9671-10
Digits Only 0143967110
Product NDC 0143-9671
Description

10 VIAL in 1 CARTON (0143-9671-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9671-01)

Marketing

Marketing Status
Marketed Since 2011-10-26
Brand cefotetan
Generic cefotetan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "239c7e32-be35-41ea-b466-2e15d3339398", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["48SPP0PA9Q"], "rxcui": ["1722919", "1722921"], "spl_set_id": ["33b13b93-58ce-44c7-b9a2-af3b3a333f80"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9671-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9671-01)", "package_ndc": "0143-9671-10", "marketing_start_date": "20111026"}], "brand_name": "Cefotetan", "product_id": "0143-9671_239c7e32-be35-41ea-b466-2e15d3339398", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9671", "generic_name": "Cefotetan", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefotetan", "active_ingredients": [{"name": "CEFOTETAN", "strength": "2 g/1"}], "application_number": "ANDA091031", "marketing_category": "ANDA", "marketing_start_date": "20111026", "listing_expiration_date": "20261231"}