Product NDC: | 10337-669 |
Proprietary Name: | Rosula |
Non Proprietary Name: | sodium sulfacetamide and sulfur |
Active Ingredient(s): | 100; 40 mg/g; mg/g & nbsp; sodium sulfacetamide and sulfur |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10337-669 |
Labeler Name: | PharmaDerm, A division of Nycomed US Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100803 |
Package NDC: | 10337-669-99 |
Package Description: | 1 CAN in 1 CARTON (10337-669-99) > 100 g in 1 CAN |
NDC Code | 10337-669-99 |
Proprietary Name | Rosula |
Package Description | 1 CAN in 1 CARTON (10337-669-99) > 100 g in 1 CAN |
Product NDC | 10337-669 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sodium sulfacetamide and sulfur |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20100803 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | PharmaDerm, A division of Nycomed US Inc. |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 100; 40 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |