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Ceftazidime and Dextrose - 0264-3143-11 - (CEFTAZIDIME)

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Drug Information of Ceftazidime and Dextrose

Product NDC: 0264-3143
Proprietary Name: Ceftazidime and Dextrose
Non Proprietary Name: CEFTAZIDIME
Active Ingredient(s): 1    g/50mL & nbsp;   CEFTAZIDIME
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ceftazidime and Dextrose

Product NDC: 0264-3143
Labeler Name: B. Braun Medical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050823
Marketing Category: NDA
Start Marketing Date: 20110613

Package Information of Ceftazidime and Dextrose

Package NDC: 0264-3143-11
Package Description: 24 CONTAINER in 1 CASE (0264-3143-11) > 50 mL in 1 CONTAINER

NDC Information of Ceftazidime and Dextrose

NDC Code 0264-3143-11
Proprietary Name Ceftazidime and Dextrose
Package Description 24 CONTAINER in 1 CASE (0264-3143-11) > 50 mL in 1 CONTAINER
Product NDC 0264-3143
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFTAZIDIME
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110613
Marketing Category Name NDA
Labeler Name B. Braun Medical Inc.
Substance Name CEFTAZIDIME
Strength Number 1
Strength Unit g/50mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftazidime and Dextrose


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