Product NDC: | 42808-111 |
Proprietary Name: | Sodium Sulfacetamide, Sulfur |
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): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42808-111 |
Labeler Name: | Exact-Rx, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110801 |
Package NDC: | 42808-111-45 |
Package Description: | 1 TUBE in 1 CARTON (42808-111-45) > 45 g in 1 TUBE |
NDC Code | 42808-111-45 |
Proprietary Name | Sodium Sulfacetamide, Sulfur |
Package Description | 1 TUBE in 1 CARTON (42808-111-45) > 45 g in 1 TUBE |
Product NDC | 42808-111 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Sulfacetamide, Sulfur |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20110801 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Exact-Rx, Inc. |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 100; 50 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |