FdaApplication
NDA 021864
Identifiers
- fda_app_no: NDA021864
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2007-05-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LYBREL | ETHINYL ESTRADIOL; LEVONORGESTREL | 0.02MG;0.09MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product