Package 0143-9976-03

Brand: cefuroxime

Generic: cefuroxime
NDC Package

Package Facts

Identity

Package NDC 0143-9976-03
Digits Only 0143997603
Product NDC 0143-9976
Product ID 0143-9976_5621cde0-74c5-45b2-8f76-329eb22b4a0a
Description

10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0143-9976-03) / 82.5 mL in 1 VIAL, PHARMACY BULK PACKAGE (0143-9976-91)

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": "5621cde0-74c5-45b2-8f76-329eb22b4a0a", "openfda": {"unii": ["R8A7M9MY61"], "rxcui": ["309101"], "spl_set_id": ["65daa2aa-cc4a-4eba-b7dc-7a151806865a"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0143-9976-03)  / 82.5 mL in 1 VIAL, PHARMACY BULK PACKAGE (0143-9976-91)", "package_ndc": "0143-9976-03", "marketing_start_date": "20040109"}], "brand_name": "Cefuroxime", "product_id": "0143-9976_5621cde0-74c5-45b2-8f76-329eb22b4a0a", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9976", "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/8mL"}], "application_number": "ANDA065046", "marketing_category": "ANDA", "marketing_start_date": "20040109", "listing_expiration_date": "20261231"}