FdaApplication
ANDA 075256
Identifiers
- fda_app_no: ANDA075256
Properties
| Property | Value |
|---|---|
| applicant_name | DURAMED PHARMACEUTICALS INC SUB BARR LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1999-08-12 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DESOGESTREL AND ETHINYL ESTRADIOL | DESOGESTREL; ETHINYL ESTRADIOL | 0.15MG;0.03MG | TABLET;ORAL-28 |
| DESOGESTREL AND ETHINYL ESTRADIOL | DESOGESTREL; ETHINYL ESTRADIOL | 0.15MG;0.03MG | TABLET;ORAL-21 |
2 products