FORTAZ - 0173-0435-00 - (ceftazidime)

Alphabetical Index


Drug Information of FORTAZ

Product NDC: 0173-0435
Proprietary Name: FORTAZ
Non Proprietary Name: ceftazidime
Active Ingredient(s): 20    mg/mL & nbsp;   ceftazidime
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of FORTAZ

Product NDC: 0173-0435
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050578
Marketing Category: NDA
Start Marketing Date: 19920813

Package Information of FORTAZ

Package NDC: 0173-0435-00
Package Description: 10 VIAL in 1 TRAY (0173-0435-00) > 18 mL in 1 VIAL

NDC Information of FORTAZ

NDC Code 0173-0435-00
Proprietary Name FORTAZ
Package Description 10 VIAL in 1 TRAY (0173-0435-00) > 18 mL in 1 VIAL
Product NDC 0173-0435
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ceftazidime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19920813
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name CEFTAZIDIME SODIUM
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of FORTAZ


General Information