| 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] |