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Gentamicin Sulfate
Gentamicin Sulfate - 0409-3400-01 - (GENTAMICIN SULFATE)
Drug Information of Gentamicin Sulfate
| Product NDC: | 0409-3400 |
| Proprietary Name: | Gentamicin Sulfate |
| Non Proprietary Name: | GENTAMICIN SULFATE |
| Active Ingredient(s): | 10 mg/mL & nbsp; GENTAMICIN SULFATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gentamicin Sulfate
| Product NDC: | 0409-3400 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062612 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111130 |
Package Information of Gentamicin Sulfate
| Package NDC: | 0409-3400-01 |
| Package Description: | 25 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-3400-01) > 6 mL in 1 VIAL, PATENT DELIVERY SYSTEM |
NDC Information of Gentamicin Sulfate
| NDC Code | 0409-3400-01 |
| Proprietary Name | Gentamicin Sulfate |
| Package Description | 25 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-3400-01) > 6 mL in 1 VIAL, PATENT DELIVERY SYSTEM |
| Product NDC | 0409-3400 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GENTAMICIN SULFATE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111130 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
