Product NDC: | 54569-1139 |
Proprietary Name: | SELENIUM SULFIDE |
Non Proprietary Name: | SELENIUM SULFIDE |
Active Ingredient(s): | 2.5 mg/100mL & nbsp; SELENIUM SULFIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-1139 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089996 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060925 |
Package NDC: | 54569-1139-0 |
Package Description: | 120 mL in 1 BOTTLE (54569-1139-0) |
NDC Code | 54569-1139-0 |
Proprietary Name | SELENIUM SULFIDE |
Package Description | 120 mL in 1 BOTTLE (54569-1139-0) |
Product NDC | 54569-1139 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SELENIUM SULFIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20060925 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | SELENIUM SULFIDE |
Strength Number | 2.5 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |