Product NDC: | 0338-1301 |
Proprietary Name: | Cefepime |
Non Proprietary Name: | cefepime |
Active Ingredient(s): | 1 g/50mL & nbsp; cefepime |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0338-1301 |
Labeler Name: | Baxter Healthcare Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050817 |
Marketing Category: | NDA |
Start Marketing Date: | 20080805 |
Package NDC: | 0338-1301-48 |
Package Description: | 12 BAG in 1 BOX (0338-1301-48) > 100 mL in 1 BAG |
NDC Code | 0338-1301-48 |
Proprietary Name | Cefepime |
Package Description | 12 BAG in 1 BOX (0338-1301-48) > 100 mL in 1 BAG |
Product NDC | 0338-1301 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | cefepime |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20080805 |
Marketing Category Name | NDA |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | CEFEPIME HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | g/50mL |
Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |