Package 0143-9568-25

Brand: cefuroxime

Generic: cefuroxime
NDC Package

Package Facts

Identity

Package NDC 0143-9568-25
Digits Only 0143956825
Product NDC 0143-9568
Product ID 0143-9568_e43d5edd-fd78-43d3-b8d2-4b22b7541042
Description

25 VIAL in 1 CARTON (0143-9568-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9568-01)

Marketing

Marketing Status
Marketed Since 2004-01-09
Brand cefuroxime
Generic cefuroxime
Sample Package No

Linked Drug Pages (1)

Cefuroxime ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "e43d5edd-fd78-43d3-b8d2-4b22b7541042", "openfda": {"unii": ["R8A7M9MY61"], "rxcui": ["1665444", "1665449"], "spl_set_id": ["19902965-d2d6-433f-982d-0095014df4e8"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0143-9568-25)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9568-01)", "package_ndc": "0143-9568-25", "marketing_start_date": "20040109"}], "brand_name": "Cefuroxime", "product_id": "0143-9568_e43d5edd-fd78-43d3-b8d2-4b22b7541042", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9568", "generic_name": "Cefuroxime", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime", "active_ingredients": [{"name": "CEFUROXIME SODIUM", "strength": "750 mg/1"}], "application_number": "ANDA065048", "marketing_category": "ANDA", "marketing_start_date": "20040109", "listing_expiration_date": "20261231"}