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Cefuroxime and Dextrose - 0264-3114-11 - (CEFUROXIME AND DEXTROSE)

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Drug Information of Cefuroxime and Dextrose

Product NDC: 0264-3114
Proprietary Name: Cefuroxime and Dextrose
Non Proprietary Name: CEFUROXIME AND DEXTROSE
Active Ingredient(s): 1.5    g/50mL & nbsp;   CEFUROXIME AND DEXTROSE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefuroxime and Dextrose

Product NDC: 0264-3114
Labeler Name: B. Braun Medical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050780
Marketing Category: NDA
Start Marketing Date: 20010221

Package Information of Cefuroxime and Dextrose

Package NDC: 0264-3114-11
Package Description: 24 CONTAINER in 1 CASE (0264-3114-11) > 50 mL in 1 CONTAINER

NDC Information of Cefuroxime and Dextrose

NDC Code 0264-3114-11
Proprietary Name Cefuroxime and Dextrose
Package Description 24 CONTAINER in 1 CASE (0264-3114-11) > 50 mL in 1 CONTAINER
Product NDC 0264-3114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFUROXIME AND DEXTROSE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20010221
Marketing Category Name NDA
Labeler Name B. Braun Medical Inc.
Substance Name CEFUROXIME SODIUM
Strength Number 1.5
Strength Unit g/50mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefuroxime and Dextrose


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