Product NDC: | 0145-0021 |
Proprietary Name: | LUXIQ |
Non Proprietary Name: | betamethasone valerate |
Active Ingredient(s): | 1.2 mg/g & nbsp; betamethasone valerate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0145-0021 |
Labeler Name: | Stiefel Laboratories Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020934 |
Marketing Category: | NDA |
Start Marketing Date: | 20091016 |
Package NDC: | 0145-0021-00 |
Package Description: | 1 CAN in 1 CARTON (0145-0021-00) > 100 g in 1 CAN |
NDC Code | 0145-0021-00 |
Proprietary Name | LUXIQ |
Package Description | 1 CAN in 1 CARTON (0145-0021-00) > 100 g in 1 CAN |
Product NDC | 0145-0021 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | betamethasone valerate |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20091016 |
Marketing Category Name | NDA |
Labeler Name | Stiefel Laboratories Inc |
Substance Name | BETAMETHASONE VALERATE |
Strength Number | 1.2 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |