Product NDC: | 43538-130 |
Proprietary Name: | Sumaxin |
Non Proprietary Name: | sodium sulfacetamide 9%-sulfur 4% |
Active Ingredient(s): | 90; 40 mg/g; mg/g & nbsp; sodium sulfacetamide 9%-sulfur 4% |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43538-130 |
Labeler Name: | Medimetriks Pharmaceutical inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED OTHER |
Start Marketing Date: | 20091030 |
Package NDC: | 43538-130-99 |
Package Description: | 12 g in 1 BOTTLE (43538-130-99) |
NDC Code | 43538-130-99 |
Proprietary Name | Sumaxin |
Package Description | 12 g in 1 BOTTLE (43538-130-99) |
Product NDC | 43538-130 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sodium sulfacetamide 9%-sulfur 4% |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20091030 |
Marketing Category Name | UNAPPROVED OTHER |
Labeler Name | Medimetriks Pharmaceutical inc |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 90; 40 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |