Product NDC: | 0462-0392 |
Proprietary Name: | LoKara |
Non Proprietary Name: | desonide |
Active Ingredient(s): | .5 mg/mL & nbsp; desonide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0462-0392 |
Labeler Name: | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA075860 |
Marketing Category: | NDA |
Start Marketing Date: | 20020319 |
Package NDC: | 0462-0392-02 |
Package Description: | 1 BOTTLE in 1 CARTON (0462-0392-02) > 59 mL in 1 BOTTLE |
NDC Code | 0462-0392-02 |
Proprietary Name | LoKara |
Package Description | 1 BOTTLE in 1 CARTON (0462-0392-02) > 59 mL in 1 BOTTLE |
Product NDC | 0462-0392 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | desonide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20020319 |
Marketing Category Name | NDA |
Labeler Name | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
Substance Name | DESONIDE |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |