Product NDC: | 42792-107 |
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): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42792-107 |
Labeler Name: | AUSTIN PHARMACEUTICALS, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110604 |
Package NDC: | 42792-107-01 |
Package Description: | 30 g in 1 BOTTLE (42792-107-01) |
NDC Code | 42792-107-01 |
Proprietary Name | SODIUM SULFACETAMIDE, SULFUR |
Package Description | 30 g in 1 BOTTLE (42792-107-01) |
Product NDC | 42792-107 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM SULFACETAMIDE, SULFUR |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110604 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | AUSTIN 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] |