FdaApplication
NDA 019192
Identifiers
- fda_app_no: NDA019192
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH PHARMACEUTICALS LLC |
| application_type | NDA |
| approval_date | 1984-11-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TRIPHASIL-21 | ETHINYL ESTRADIOL; LEVONORGESTREL | 0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL-21 |
1 product