Product NDC: | 76439-321 |
Proprietary Name: | Virti-SULF |
Non Proprietary Name: | SULFACETAMIDE SODIUM AND SULFUR |
Active Ingredient(s): | 100; 50 mg/g; mg/g & nbsp; SULFACETAMIDE SODIUM AND SULFUR |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76439-321 |
Labeler Name: | Virtus Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120912 |
Package NDC: | 76439-321-01 |
Package Description: | 28 g in 1 TUBE (76439-321-01) |
NDC Code | 76439-321-01 |
Proprietary Name | Virti-SULF |
Package Description | 28 g in 1 TUBE (76439-321-01) |
Product NDC | 76439-321 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SULFACETAMIDE SODIUM AND SULFUR |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120912 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Virtus Pharmaceuticals |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 100; 50 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |