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Sulfacetamide Sodium, Sulfur
Sulfacetamide Sodium, Sulfur - 67877-268-17 - (Sulfacetamide Sodium, Sulfur)
Drug Information of Sulfacetamide Sodium, Sulfur
| Product NDC: | 67877-268 |
| Proprietary Name: | Sulfacetamide Sodium, Sulfur |
| Non Proprietary Name: | Sulfacetamide Sodium, Sulfur |
| Active Ingredient(s): | 100; 50 mg/g; mg/g & nbsp; Sulfacetamide Sodium, Sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulfacetamide Sodium, Sulfur
| Product NDC: | 67877-268 |
| Labeler Name: | Ascend Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20111108 |
Package Information of Sulfacetamide Sodium, Sulfur
| Package NDC: | 67877-268-17 |
| Package Description: | 170.1 g in 1 TUBE (67877-268-17) |
NDC Information of Sulfacetamide Sodium, Sulfur
| NDC Code | 67877-268-17 |
| Proprietary Name | Sulfacetamide Sodium, Sulfur |
| Package Description | 170.1 g in 1 TUBE (67877-268-17) |
| Product NDC | 67877-268 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sulfacetamide Sodium, Sulfur |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111108 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Ascend Laboratories, LLC |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 100; 50 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
