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] |