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SODIUM SULFACETAMIDE, SULFUR
SODIUM SULFACETAMIDE, SULFUR - 42792-103-01 - (SODIUM SULFACETAMIDE, SULFUR)
Drug Information of SODIUM SULFACETAMIDE, SULFUR
| Product NDC: | 42792-103 |
| Proprietary Name: | SODIUM SULFACETAMIDE, SULFUR |
| Non Proprietary Name: | SODIUM SULFACETAMIDE, SULFUR |
| Active Ingredient(s): | 100; 50 mg/g; mg/g & nbsp; SODIUM SULFACETAMIDE, SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SODIUM SULFACETAMIDE, SULFUR
| Product NDC: | 42792-103 |
| Labeler Name: | AUSTIN PHARMACEUTICALS, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110430 |
Package Information of SODIUM SULFACETAMIDE, SULFUR
| Package NDC: | 42792-103-01 |
| Package Description: | 28 g in 1 BOTTLE (42792-103-01) |
NDC Information of SODIUM SULFACETAMIDE, SULFUR
| NDC Code | 42792-103-01 |
| Proprietary Name | SODIUM SULFACETAMIDE, SULFUR |
| Package Description | 28 g in 1 BOTTLE (42792-103-01) |
| Product NDC | 42792-103 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM SULFACETAMIDE, SULFUR |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110430 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | AUSTIN PHARMACEUTICALS, LLC |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 100; 50 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
