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Ceftazidime - 44567-235-25 - (Ceftazidime)

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Drug Information of Ceftazidime

Product NDC: 44567-235
Proprietary Name: Ceftazidime
Non Proprietary Name: Ceftazidime
Active Ingredient(s): 1    g/20mL & nbsp;   Ceftazidime
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ceftazidime

Product NDC: 44567-235
Labeler Name: WG Critical Care, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062640
Marketing Category: ANDA
Start Marketing Date: 20130131

Package Information of Ceftazidime

Package NDC: 44567-235-25
Package Description: 25 VIAL in 1 CARTON (44567-235-25) > 20 mL in 1 VIAL

NDC Information of Ceftazidime

NDC Code 44567-235-25
Proprietary Name Ceftazidime
Package Description 25 VIAL in 1 CARTON (44567-235-25) > 20 mL in 1 VIAL
Product NDC 44567-235
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftazidime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20130131
Marketing Category Name ANDA
Labeler Name WG Critical Care, LLC
Substance Name CEFTAZIDIME
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftazidime


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