| Product NDC: | 39822-0330 |
| Proprietary Name: | Neo-Fradin |
| Non Proprietary Name: | Neomycin Sulfate |
| Active Ingredient(s): | 87.5 mg/5mL & nbsp; Neomycin Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 39822-0330 |
| Labeler Name: | X-GEN Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065010 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020523 |
| Package NDC: | 39822-0330-2 |
| Package Description: | 59 mL in 1 BOTTLE (39822-0330-2) |
| NDC Code | 39822-0330-2 |
| Proprietary Name | Neo-Fradin |
| Package Description | 59 mL in 1 BOTTLE (39822-0330-2) |
| Product NDC | 39822-0330 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Neomycin Sulfate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20020523 |
| Marketing Category Name | ANDA |
| Labeler Name | X-GEN Pharmaceuticals, Inc. |
| Substance Name | NEOMYCIN SULFATE |
| Strength Number | 87.5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |