Product NDC: | 0009-5137 |
Proprietary Name: | Zyvox |
Non Proprietary Name: | linezolid |
Active Ingredient(s): | 200 mg/100mL & nbsp; linezolid |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0009-5137 |
Labeler Name: | Pharmacia and Upjohn Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021131 |
Marketing Category: | NDA |
Start Marketing Date: | 20000418 |
Package NDC: | 0009-5137-01 |
Package Description: | 100 mL in 1 BAG (0009-5137-01) |
NDC Code | 0009-5137-01 |
Proprietary Name | Zyvox |
Package Description | 100 mL in 1 BAG (0009-5137-01) |
Product NDC | 0009-5137 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | linezolid |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20000418 |
Marketing Category Name | NDA |
Labeler Name | Pharmacia and Upjohn Company |
Substance Name | LINEZOLID |
Strength Number | 200 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Oxazolidinone Antibacterial [EPC],Oxazolidinones [Chemical/Ingredient] |