Product NDC: | 0591-0810 |
Proprietary Name: | Silver Sulfadiazene |
Non Proprietary Name: | Silver Sulfadiazine |
Active Ingredient(s): | 10 g/1000g & nbsp; Silver Sulfadiazine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0591-0810 |
Labeler Name: | Watson Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018578 |
Marketing Category: | NDA |
Start Marketing Date: | 19820225 |
Package NDC: | 0591-0810-55 |
Package Description: | 50 g in 1 JAR (0591-0810-55) |
NDC Code | 0591-0810-55 |
Proprietary Name | Silver Sulfadiazene |
Package Description | 50 g in 1 JAR (0591-0810-55) |
Product NDC | 0591-0810 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Silver Sulfadiazine |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19820225 |
Marketing Category Name | NDA |
Labeler Name | Watson Laboratories, Inc. |
Substance Name | SILVER SULFADIAZINE |
Strength Number | 10 |
Strength Unit | g/1000g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |