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