Home
>
National Drug Code (NDC)
>
Sumaxin
Sumaxin - 43538-160-16 - (Sodium Sulfacetamide and Sulfur)
Drug Information of Sumaxin
| Product NDC: | 43538-160 |
| Proprietary Name: | Sumaxin |
| Non Proprietary Name: | Sodium Sulfacetamide and Sulfur |
| Active Ingredient(s): | 80; 40 mg/mL; mg/mL & nbsp; Sodium Sulfacetamide and Sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sumaxin
| Product NDC: | 43538-160 |
| Labeler Name: | Medimetriks Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100902 |
Package Information of Sumaxin
| Package NDC: | 43538-160-16 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (43538-160-16) > 473 mL in 1 BOTTLE, PUMP |
NDC Information of Sumaxin
| NDC Code | 43538-160-16 |
| Proprietary Name | Sumaxin |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (43538-160-16) > 473 mL in 1 BOTTLE, PUMP |
| Product NDC | 43538-160 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Sulfacetamide and Sulfur |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100902 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Medimetriks Pharmaceuticals, Inc. |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 80; 40 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
