FdaApplication
ANDA 075406
Identifiers
- fda_app_no: ANDA075406
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1999-12-15 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OGESTREL 0.5/50-21 | ETHINYL ESTRADIOL; NORGESTREL | 0.05MG;0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL-21 |
| OGESTREL 0.5/50-28 | ETHINYL ESTRADIOL; NORGESTREL | 0.05MG;0.5MG | TABLET;ORAL-28 |
2 products