Product NDC: | 54868-6225 |
Proprietary Name: | Sulfacetamide Sodium |
Non Proprietary Name: | Sulfacetamide Sodium |
Active Ingredient(s): | 100 mg/mL & nbsp; Sulfacetamide Sodium |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6225 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077015 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110119 |
Package NDC: | 54868-6225-0 |
Package Description: | 1 BOTTLE in 1 CARTON (54868-6225-0) > 118 mL in 1 BOTTLE |
NDC Code | 54868-6225-0 |
Proprietary Name | Sulfacetamide Sodium |
Package Description | 1 BOTTLE in 1 CARTON (54868-6225-0) > 118 mL in 1 BOTTLE |
Product NDC | 54868-6225 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sulfacetamide Sodium |
Dosage Form Name | SUSPENSION |
Route Name | TOPICAL |
Start Marketing Date | 20110119 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | SULFACETAMIDE SODIUM |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |