FdaApplication
NDA 210566
Identifiers
- fda_app_no: NDA210566
Properties
| Property | Value |
|---|---|
| applicant_name | MAYNE PHARMA LLC |
| application_type | NDA |
| approval_date | 2018-05-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LEXETTE | HALOBETASOL PROPIONATE | 0.05% | AEROSOL, FOAM;TOPICAL |
1 product