| 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] |