Product NDC: | 21695-584 |
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: | 21695-584 |
Labeler Name: | Rebel Distributors Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070062 |
Marketing Category: | ANDA |
Start Marketing Date: | 19850514 |
Package NDC: | 21695-584-15 |
Package Description: | 1 TUBE in 1 CARTON (21695-584-15) > 15 g in 1 TUBE |
NDC Code | 21695-584-15 |
Proprietary Name | Betamethasone Valerate |
Package Description | 1 TUBE in 1 CARTON (21695-584-15) > 15 g in 1 TUBE |
Product NDC | 21695-584 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Betamethasone Valerate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19850514 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp. |
Substance Name | BETAMETHASONE VALERATE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |