Product NDC: | 45802-942 |
Proprietary Name: | sodium sulfacetamide 10 and sulfur 5 |
Non Proprietary Name: | Sodium Sulfacetamide, Sulfur |
Active Ingredient(s): | 100; 50 mg/g; mg/g & nbsp; Sodium Sulfacetamide, Sulfur |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45802-942 |
Labeler Name: | Perrigo New York Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20080606 |
Package NDC: | 45802-942-02 |
Package Description: | 2 TUBE in 1 CARTON (45802-942-02) > 170.1 g in 1 TUBE |
NDC Code | 45802-942-02 |
Proprietary Name | sodium sulfacetamide 10 and sulfur 5 |
Package Description | 2 TUBE in 1 CARTON (45802-942-02) > 170.1 g in 1 TUBE |
Product NDC | 45802-942 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Sulfacetamide, Sulfur |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20080606 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Perrigo New York Inc |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 100; 50 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |