Product NDC: | 13925-114 |
Proprietary Name: | SE 10-5 SS |
Non Proprietary Name: | SODIUM SULFACETAMIDE, SULFUR |
Active Ingredient(s): | 100; 50 mg/g; mg/g & nbsp; SODIUM SULFACETAMIDE, SULFUR |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13925-114 |
Labeler Name: | Seton Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100515 |
Package NDC: | 13925-114-04 |
Package Description: | 1 TUBE in 1 CARTON (13925-114-04) > 113.4 g in 1 TUBE |
NDC Code | 13925-114-04 |
Proprietary Name | SE 10-5 SS |
Package Description | 1 TUBE in 1 CARTON (13925-114-04) > 113.4 g in 1 TUBE |
Product NDC | 13925-114 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM SULFACETAMIDE, SULFUR |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100515 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Seton Pharmaceuticals |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 100; 50 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |