| Product NDC: | 51079-624 |
| Proprietary Name: | Sulfamylon |
| Non Proprietary Name: | mafenide acetate |
| Active Ingredient(s): | 50 g/1 & nbsp; mafenide acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51079-624 |
| Labeler Name: | Mylan Institutional Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019832 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120228 |
| Package NDC: | 51079-624-85 |
| Package Description: | 5 PACKET in 1 CARTON (51079-624-85) > 1 POWDER, FOR SOLUTION in 1 PACKET (51079-624-84) (51079-624-84) |
| NDC Code | 51079-624-85 |
| Proprietary Name | Sulfamylon |
| Package Description | 5 PACKET in 1 CARTON (51079-624-85) > 1 POWDER, FOR SOLUTION in 1 PACKET (51079-624-84) (51079-624-84) |
| Product NDC | 51079-624 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | mafenide acetate |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120228 |
| Marketing Category Name | NDA |
| Labeler Name | Mylan Institutional Inc. |
| Substance Name | MAFENIDE ACETATE |
| Strength Number | 50 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Methylated Sulfonamide Antibacterial [EPC],Methylated Sulfonamides [Chemical/Ingredient] |