Package 0143-9569-10

Brand: cefuroxime

Generic: cefuroxime
NDC Package

Package Facts

Identity

Package NDC 0143-9569-10
Digits Only 0143956910
Product NDC 0143-9569
Product ID 0143-9569_a44c47cd-1104-4275-b859-d7ed2af78b8e
Description

10 VIAL in 1 CARTON (0143-9569-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9569-01)

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": ["INTRAVENOUS"], "spl_id": "a44c47cd-1104-4275-b859-d7ed2af78b8e", "openfda": {"unii": ["R8A7M9MY61"], "rxcui": ["309101"], "spl_set_id": ["79f5cf6f-a5e2-49a2-9704-fa1bd21338c3"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9569-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9569-01)", "package_ndc": "0143-9569-10", "marketing_start_date": "20040109"}], "brand_name": "Cefuroxime", "product_id": "0143-9569_a44c47cd-1104-4275-b859-d7ed2af78b8e", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9569", "generic_name": "Cefuroxime", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime", "active_ingredients": [{"name": "CEFUROXIME SODIUM", "strength": "7.5 g/1"}], "application_number": "ANDA065046", "marketing_category": "ANDA", "marketing_start_date": "20040109", "listing_expiration_date": "20261231"}