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Sodium Sulfacetamide and Sulfur
Sodium Sulfacetamide and Sulfur - 13925-161-12 - (Sodium Sulfacetamide and Sulfur)
Drug Information of Sodium Sulfacetamide and Sulfur
| Product NDC: | 13925-161 |
| Proprietary Name: | Sodium Sulfacetamide and Sulfur |
| Non Proprietary Name: | Sodium Sulfacetamide and Sulfur |
| Active Ingredient(s): | 100; 50 mg/mL; mg/mL & nbsp; Sodium Sulfacetamide and Sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Sulfacetamide and Sulfur
| Product NDC: | 13925-161 |
| Labeler Name: | Seton Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110527 |
Package Information of Sodium Sulfacetamide and Sulfur
| Package NDC: | 13925-161-12 |
| Package Description: | 355 mL in 1 BOTTLE (13925-161-12) |
NDC Information of Sodium Sulfacetamide and Sulfur
| NDC Code | 13925-161-12 |
| Proprietary Name | Sodium Sulfacetamide and Sulfur |
| Package Description | 355 mL in 1 BOTTLE (13925-161-12) |
| Product NDC | 13925-161 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Sulfacetamide and Sulfur |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110527 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Seton Pharmaceuticals |
| Substance Name | SULFACETAMIDE; SULFUR |
| Strength Number | 100; 50 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
