 
                        | Product NDC: | 0904-5941 | 
| Proprietary Name: | Neomycin Sulfate | 
| Non Proprietary Name: | Neomycin Sulfate | 
| Active Ingredient(s): | 500 mg/1 & nbsp; Neomycin Sulfate | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0904-5941 | 
| Labeler Name: | Major Pharmaceuticals | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA060304 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20090914 | 
| Package NDC: | 0904-5941-06 | 
| Package Description: | 50 TABLET in 1 BOX, UNIT-DOSE (0904-5941-06) | 
| NDC Code | 0904-5941-06 | 
| Proprietary Name | Neomycin Sulfate | 
| Package Description | 50 TABLET in 1 BOX, UNIT-DOSE (0904-5941-06) | 
| Product NDC | 0904-5941 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Neomycin Sulfate | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20090914 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Major Pharmaceuticals | 
| Substance Name | NEOMYCIN SULFATE | 
| Strength Number | 500 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |