| Product NDC: | 17478-290 |
| Proprietary Name: | Tobramycin |
| Non Proprietary Name: | Tobramycin |
| Active Ingredient(s): | 3 mg/mL & nbsp; Tobramycin |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 17478-290 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064096 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960131 |
| Package NDC: | 17478-290-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-290-10) > 5 mL in 1 BOTTLE, DROPPER |
| NDC Code | 17478-290-10 |
| Proprietary Name | Tobramycin |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-290-10) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-290 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tobramycin |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19960131 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | TOBRAMYCIN |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |