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Cefoxitin and Dextrose - 0264-3125-11 - (CEFOXITIN SODIUM)

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Drug Information of Cefoxitin and Dextrose

Product NDC: 0264-3125
Proprietary Name: Cefoxitin and Dextrose
Non Proprietary Name: CEFOXITIN SODIUM
Active Ingredient(s): 2    g/50mL & nbsp;   CEFOXITIN SODIUM
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefoxitin and Dextrose

Product NDC: 0264-3125
Labeler Name: B. Braun Medical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA065214
Marketing Category: NDA
Start Marketing Date: 20060310

Package Information of Cefoxitin and Dextrose

Package NDC: 0264-3125-11
Package Description: 24 CONTAINER in 1 CASE (0264-3125-11) > 50 mL in 1 CONTAINER

NDC Information of Cefoxitin and Dextrose

NDC Code 0264-3125-11
Proprietary Name Cefoxitin and Dextrose
Package Description 24 CONTAINER in 1 CASE (0264-3125-11) > 50 mL in 1 CONTAINER
Product NDC 0264-3125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFOXITIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20060310
Marketing Category Name NDA
Labeler Name B. Braun Medical Inc.
Substance Name CEFOXITIN SODIUM
Strength Number 2
Strength Unit g/50mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefoxitin and Dextrose


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