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SODIUM SULFACETAMIDE - SULFUR WASH
SODIUM SULFACETAMIDE - SULFUR WASH - 42192-121-16 - (SODIUM SULFACETAMIDE, SULFUR)
Drug Information of SODIUM SULFACETAMIDE - SULFUR WASH
| Product NDC: | 42192-121 |
| Proprietary Name: | SODIUM SULFACETAMIDE - SULFUR WASH |
| Non Proprietary Name: | SODIUM SULFACETAMIDE, SULFUR |
| Active Ingredient(s): | 90; 40 mg/473.2mL; mg/473.2mL & nbsp; SODIUM SULFACETAMIDE, SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SODIUM SULFACETAMIDE - SULFUR WASH
| Product NDC: | 42192-121 |
| Labeler Name: | ACELLA PHARMACEUTICALS |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100916 |
Package Information of SODIUM SULFACETAMIDE - SULFUR WASH
| Package NDC: | 42192-121-16 |
| Package Description: | 473.2 mL in 1 BOTTLE (42192-121-16) |
NDC Information of SODIUM SULFACETAMIDE - SULFUR WASH
| NDC Code | 42192-121-16 |
| Proprietary Name | SODIUM SULFACETAMIDE - SULFUR WASH |
| Package Description | 473.2 mL in 1 BOTTLE (42192-121-16) |
| Product NDC | 42192-121 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM SULFACETAMIDE, SULFUR |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100916 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | ACELLA PHARMACEUTICALS |
| Substance Name | SULFACETAMIDE; SULFUR |
| Strength Number | 90; 40 |
| Strength Unit | mg/473.2mL; mg/473.2mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
