Product NDC: | 21695-182 |
Proprietary Name: | Thermazene |
Non Proprietary Name: | Silver Sulfadiazine |
Active Ingredient(s): | 10 mg/g & nbsp; Silver Sulfadiazine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-182 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018810 |
Marketing Category: | NDA |
Start Marketing Date: | 19851223 |
Package NDC: | 21695-182-50 |
Package Description: | 50 g in 1 TUBE (21695-182-50) |
NDC Code | 21695-182-50 |
Proprietary Name | Thermazene |
Package Description | 50 g in 1 TUBE (21695-182-50) |
Product NDC | 21695-182 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Silver Sulfadiazine |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19851223 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | SILVER SULFADIAZINE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |