Product NDC: | 52125-445 |
Proprietary Name: | Betamethasone Valerate |
Non Proprietary Name: | betamethasone valerate |
Active Ingredient(s): | 1 mg/g & nbsp; betamethasone valerate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52125-445 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018861 |
Marketing Category: | NDA |
Start Marketing Date: | 20130610 |
Package NDC: | 52125-445-01 |
Package Description: | 15 g in 1 TUBE (52125-445-01) |
NDC Code | 52125-445-01 |
Proprietary Name | Betamethasone Valerate |
Package Description | 15 g in 1 TUBE (52125-445-01) |
Product NDC | 52125-445 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | betamethasone valerate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130610 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | BETAMETHASONE VALERATE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |