Product NDC: | 0168-0382 |
Proprietary Name: | Sulfacetamide Sodium |
Non Proprietary Name: | Sulfacetamide Sodium |
Active Ingredient(s): | 100 mg/mL & nbsp; Sulfacetamide Sodium |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0168-0382 |
Labeler Name: | E. Fougera & CO. a division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077015 |
Marketing Category: | ANDA |
Start Marketing Date: | 20061117 |
Package NDC: | 0168-0382-04 |
Package Description: | 118 mL in 1 BOTTLE (0168-0382-04) |
NDC Code | 0168-0382-04 |
Proprietary Name | Sulfacetamide Sodium |
Package Description | 118 mL in 1 BOTTLE (0168-0382-04) |
Product NDC | 0168-0382 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sulfacetamide Sodium |
Dosage Form Name | SUSPENSION |
Route Name | TOPICAL |
Start Marketing Date | 20061117 |
Marketing Category Name | ANDA |
Labeler Name | E. Fougera & CO. a division of Fougera Pharmaceuticals Inc. |
Substance Name | SULFACETAMIDE SODIUM |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |