Package 0264-3114-11
Brand: cefuroxime and dextrose
Generic: cefuroxime and dextrosePackage Facts
Identity
Package NDC
0264-3114-11
Digits Only
0264311411
Product NDC
0264-3114
Description
24 CONTAINER in 1 CASE (0264-3114-11) / 50 mL in 1 CONTAINER
Marketing
Marketing Status
Brand
cefuroxime and dextrose
Generic
cefuroxime and dextrose
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6874a295-7ec7-4822-9d04-4dd9932b4546", "openfda": {"unii": ["R8A7M9MY61"], "rxcui": ["1665444", "1665449"], "spl_set_id": ["07170ee3-1a24-424f-a2a2-00bc92e98f85"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 CONTAINER in 1 CASE (0264-3114-11) / 50 mL in 1 CONTAINER", "package_ndc": "0264-3114-11", "marketing_start_date": "20010221"}], "brand_name": "Cefuroxime and Dextrose", "product_id": "0264-3114_6874a295-7ec7-4822-9d04-4dd9932b4546", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0264-3114", "generic_name": "CEFUROXIME AND DEXTROSE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefuroxime and Dextrose", "active_ingredients": [{"name": "CEFUROXIME SODIUM", "strength": "1.5 g/50mL"}], "application_number": "NDA050780", "marketing_category": "NDA", "marketing_start_date": "20010221", "listing_expiration_date": "20261231"}