| Product NDC: | 45802-046 |
| Proprietary Name: | Gentamicin Sulfate |
| Non Proprietary Name: | Gentamicin Sulfate |
| Active Ingredient(s): | 1 mg/g & nbsp; Gentamicin Sulfate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 45802-046 |
| Labeler Name: | Perrigo New York Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062351 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060710 |
| Package NDC: | 45802-046-35 |
| Package Description: | 1 TUBE in 1 CARTON (45802-046-35) > 15 g in 1 TUBE |
| NDC Code | 45802-046-35 |
| Proprietary Name | Gentamicin Sulfate |
| Package Description | 1 TUBE in 1 CARTON (45802-046-35) > 15 g in 1 TUBE |
| Product NDC | 45802-046 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Gentamicin Sulfate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20060710 |
| Marketing Category Name | ANDA |
| Labeler Name | Perrigo New York Inc |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |