Product NDC: | 54569-1874 |
Proprietary Name: | Betamethasone Valerate |
Non Proprietary Name: | betamethasone valerate |
Active Ingredient(s): | 1 mg/mL & nbsp; betamethasone valerate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-1874 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018866 |
Marketing Category: | NDA |
Start Marketing Date: | 19830831 |
Package NDC: | 54569-1874-1 |
Package Description: | 60 mL in 1 BOTTLE (54569-1874-1) |
NDC Code | 54569-1874-1 |
Proprietary Name | Betamethasone Valerate |
Package Description | 60 mL in 1 BOTTLE (54569-1874-1) |
Product NDC | 54569-1874 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | betamethasone valerate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 19830831 |
Marketing Category Name | NDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | BETAMETHASONE VALERATE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |