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SODIUM SULFACETAMIDE and SULFUR
SODIUM SULFACETAMIDE and SULFUR - 42192-104-06 - (SODIUM SULFACETAMIDE and SULFUR)
Drug Information of SODIUM SULFACETAMIDE and SULFUR
| Product NDC: | 42192-104 |
| Proprietary Name: | SODIUM SULFACETAMIDE and SULFUR |
| Non Proprietary Name: | SODIUM SULFACETAMIDE and SULFUR |
| Active Ingredient(s): | 100; 10 mg/g; mg/g & nbsp; SODIUM SULFACETAMIDE and SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SODIUM SULFACETAMIDE and SULFUR
| Product NDC: | 42192-104 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20080208 |
Package Information of SODIUM SULFACETAMIDE and SULFUR
| Package NDC: | 42192-104-06 |
| Package Description: | 1 TUBE in 1 CARTON (42192-104-06) > 170.1 g in 1 TUBE |
NDC Information of SODIUM SULFACETAMIDE and SULFUR
| NDC Code | 42192-104-06 |
| Proprietary Name | SODIUM SULFACETAMIDE and SULFUR |
| Package Description | 1 TUBE in 1 CARTON (42192-104-06) > 170.1 g in 1 TUBE |
| Product NDC | 42192-104 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM SULFACETAMIDE and SULFUR |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20080208 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 100; 10 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
