| Product NDC: | 54569-1144 |
| 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: | 54569-1144 |
| Labeler Name: | A-S Medication Solutions LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062533 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100317 |
| Package NDC: | 54569-1144-0 |
| Package Description: | 15 g in 1 TUBE (54569-1144-0) |
| NDC Code | 54569-1144-0 |
| Proprietary Name | Gentamicin sulfate |
| Package Description | 15 g in 1 TUBE (54569-1144-0) |
| Product NDC | 54569-1144 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Gentamicin Sulfate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100317 |
| Marketing Category Name | ANDA |
| Labeler Name | A-S Medication Solutions LLC |
| Substance Name | GENTAMICIN |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |