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Mafenide acetate
Mafenide acetate - 49884-902-52 - (Mafenide acetate)
Drug Information of Mafenide acetate
| Product NDC: | 49884-902 |
| Proprietary Name: | Mafenide acetate |
| 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) |
Labeler Information of Mafenide acetate
| Product NDC: | 49884-902 |
| Labeler Name: | Par Pharmaceutical Companies, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201511 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130212 |
Package Information of Mafenide acetate
| Package NDC: | 49884-902-52 |
| Package Description: | 1 CARTON in 1 PACKET (49884-902-52) > 5 POWDER, FOR SOLUTION in 1 CARTON (49884-902-78) |
NDC Information of Mafenide acetate
| NDC Code | 49884-902-52 |
| Proprietary Name | Mafenide acetate |
| Package Description | 1 CARTON in 1 PACKET (49884-902-52) > 5 POWDER, FOR SOLUTION in 1 CARTON (49884-902-78) |
| Product NDC | 49884-902 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mafenide acetate |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130212 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Companies, Inc. |
| Substance Name | MAFENIDE ACETATE |
| Strength Number | 50 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Methylated Sulfonamide Antibacterial [EPC],Methylated Sulfonamides [Chemical/Ingredient] |
