Package 0143-9979-22

Brand: cefuroxime

Generic: cefuroxime
NDC Package

Package Facts

Identity

Package NDC 0143-9979-22
Digits Only 0143997922
Product NDC 0143-9979
Product ID 0143-9979_6341f645-bd5f-4d4f-a532-2c0740ab95f5
Description

25 VIAL in 1 CARTON (0143-9979-22) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9979-90)

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": "6341f645-bd5f-4d4f-a532-2c0740ab95f5", "openfda": {"unii": ["R8A7M9MY61"], "rxcui": ["1665444", "1665449"], "spl_set_id": ["703cc338-c0b6-4a02-b8db-c27aeff181df"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0143-9979-22)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9979-90)", "package_ndc": "0143-9979-22", "marketing_start_date": "20040109"}], "brand_name": "Cefuroxime", "product_id": "0143-9979_6341f645-bd5f-4d4f-a532-2c0740ab95f5", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9979", "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"}