Product NDC: | 0264-3175 |
Proprietary Name: | Cefotetan and Dextrose |
Non Proprietary Name: | CEFOTETAN and DEXTROSE |
Active Ingredient(s): | 2 g/50mL & nbsp; CEFOTETAN and DEXTROSE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0264-3175 |
Labeler Name: | B. Braun Medical Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA065430 |
Marketing Category: | NDA |
Start Marketing Date: | 20100820 |
Package NDC: | 0264-3175-11 |
Package Description: | 24 CONTAINER in 1 CASE (0264-3175-11) > 50 mL in 1 CONTAINER |
NDC Code | 0264-3175-11 |
Proprietary Name | Cefotetan and Dextrose |
Package Description | 24 CONTAINER in 1 CASE (0264-3175-11) > 50 mL in 1 CONTAINER |
Product NDC | 0264-3175 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CEFOTETAN and DEXTROSE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100820 |
Marketing Category Name | NDA |
Labeler Name | B. Braun Medical Inc. |
Substance Name | CEFOTETAN DISODIUM |
Strength Number | 2 |
Strength Unit | g/50mL |
Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |