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Tobramycin
Tobramycin - 50436-7392-1 - (Tobramycin)
Drug Information of Tobramycin
| Product NDC: | 50436-7392 |
| Proprietary Name: | Tobramycin |
| Non Proprietary Name: | Tobramycin |
| Active Ingredient(s): | 3 mg/mL & nbsp; Tobramycin |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tobramycin
| Product NDC: | 50436-7392 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062535 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950109 |
Package Information of Tobramycin
| Package NDC: | 50436-7392-1 |
| Package Description: | 5 mL in 1 BOTTLE (50436-7392-1) |
NDC Information of Tobramycin
| NDC Code | 50436-7392-1 |
| Proprietary Name | Tobramycin |
| Package Description | 5 mL in 1 BOTTLE (50436-7392-1) |
| Product NDC | 50436-7392 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tobramycin |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19950109 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | TOBRAMYCIN |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
