Product NDC: | 54295-307 |
Proprietary Name: | Sulfacetamide Sodium, Sulfur |
Non Proprietary Name: | Sulfacetamide Sodium, Sulfur |
Active Ingredient(s): | 100; 50 mg/g; mg/g & nbsp; Sulfacetamide Sodium, Sulfur |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54295-307 |
Labeler Name: | Trinity Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130701 |
Package NDC: | 54295-307-23 |
Package Description: | 170.1 g in 1 TUBE (54295-307-23) |
NDC Code | 54295-307-23 |
Proprietary Name | Sulfacetamide Sodium, Sulfur |
Package Description | 170.1 g in 1 TUBE (54295-307-23) |
Product NDC | 54295-307 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sulfacetamide Sodium, Sulfur |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130701 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Trinity Pharmaceuticals, LLC |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 100; 50 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |