Product NDC: | 0187-5198 |
Proprietary Name: | Klaron |
Non Proprietary Name: | sulfacetamide sodium |
Active Ingredient(s): | 10 mg/mL & nbsp; sulfacetamide sodium |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0187-5198 |
Labeler Name: | Valeant Pharmaceuticals North America LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019931 |
Marketing Category: | NDA |
Start Marketing Date: | 20130404 |
Package NDC: | 0187-5198-04 |
Package Description: | 118 mL in 1 BOTTLE, PLASTIC (0187-5198-04) |
NDC Code | 0187-5198-04 |
Proprietary Name | Klaron |
Package Description | 118 mL in 1 BOTTLE, PLASTIC (0187-5198-04) |
Product NDC | 0187-5198 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sulfacetamide sodium |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130404 |
Marketing Category Name | NDA |
Labeler Name | Valeant Pharmaceuticals North America LLC |
Substance Name | SULFACETAMIDE SODIUM |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |