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Tobramycin sulfate
Tobramycin sulfate - 0703-9402-04 - (Tobramycin sulfate)
Drug Information of Tobramycin sulfate
| Product NDC: | 0703-9402 |
| Proprietary Name: | Tobramycin sulfate |
| Non Proprietary Name: | Tobramycin sulfate |
| Active Ingredient(s): | 40 mg/mL & nbsp; Tobramycin sulfate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tobramycin sulfate
| Product NDC: | 0703-9402 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA063100 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19920201 |
Package Information of Tobramycin sulfate
| Package NDC: | 0703-9402-04 |
| Package Description: | 25 VIAL in 1 TRAY (0703-9402-04) > 2 mL in 1 VIAL (0703-9402-01) |
NDC Information of Tobramycin sulfate
| NDC Code | 0703-9402-04 |
| Proprietary Name | Tobramycin sulfate |
| Package Description | 25 VIAL in 1 TRAY (0703-9402-04) > 2 mL in 1 VIAL (0703-9402-01) |
| Product NDC | 0703-9402 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tobramycin sulfate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19920201 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | TOBRAMYCIN SULFATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
