Product NDC: | 42192-133 |
Proprietary Name: | Sodium Sulfacetamide and Sulfur |
Non Proprietary Name: | Sodium Sulfacetamide and Sulfur |
Active Ingredient(s): | 80; 40 mg/mL; mg/mL & nbsp; Sodium Sulfacetamide and Sulfur |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42192-133 |
Labeler Name: | Acella Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110727 |
Package NDC: | 42192-133-16 |
Package Description: | 473 mL in 1 BOTTLE (42192-133-16) |
NDC Code | 42192-133-16 |
Proprietary Name | Sodium Sulfacetamide and Sulfur |
Package Description | 473 mL in 1 BOTTLE (42192-133-16) |
Product NDC | 42192-133 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Sulfacetamide and Sulfur |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20110727 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Acella Pharmaceuticals, LLC |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 80; 40 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |