Product NDC: | 43538-100 |
Proprietary Name: | Sumaxin |
Non Proprietary Name: | sulfacetamide sodium and Sulfur |
Active Ingredient(s): | 100; 40 mg/g; mg/g & nbsp; sulfacetamide sodium and Sulfur |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CLOTH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43538-100 |
Labeler Name: | Medimetriks Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20090101 |
Package NDC: | 43538-100-60 |
Package Description: | 60 PACKET in 1 CARTON (43538-100-60) > 3.7 g in 1 PACKET |
NDC Code | 43538-100-60 |
Proprietary Name | Sumaxin |
Package Description | 60 PACKET in 1 CARTON (43538-100-60) > 3.7 g in 1 PACKET |
Product NDC | 43538-100 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sulfacetamide sodium and Sulfur |
Dosage Form Name | CLOTH |
Route Name | TOPICAL |
Start Marketing Date | 20090101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Medimetriks Pharmaceuticals, Inc. |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 100; 40 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |