FdaApplication
NDA 203159
Identifiers
- fda_app_no: NDA203159
Properties
| Property | Value |
|---|---|
| applicant_name | BAYER HEALTHCARE PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2013-01-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SKYLA | LEVONORGESTREL | 13.5MG | SYSTEM;INTRAUTERINE |
1 product