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Tobramycin
Tobramycin - 63323-303-51 - (TOBRAMYCIN SULFATE)
Drug Information of Tobramycin
| Product NDC: | 63323-303 |
| Proprietary Name: | Tobramycin |
| Non Proprietary Name: | TOBRAMYCIN SULFATE |
| Active Ingredient(s): | 1200 mg/30mL & nbsp; TOBRAMYCIN SULFATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tobramycin
| Product NDC: | 63323-303 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050789 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20051123 |
Package Information of Tobramycin
| Package NDC: | 63323-303-51 |
| Package Description: | 6 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-303-51) > 30 mL in 1 VIAL, PHARMACY BULK PACKAGE |
NDC Information of Tobramycin
| NDC Code | 63323-303-51 |
| Proprietary Name | Tobramycin |
| Package Description | 6 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-303-51) > 30 mL in 1 VIAL, PHARMACY BULK PACKAGE |
| Product NDC | 63323-303 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TOBRAMYCIN SULFATE |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20051123 |
| Marketing Category Name | NDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | TOBRAMYCIN SULFATE |
| Strength Number | 1200 |
| Strength Unit | mg/30mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
