FdaApplication
ANDA 208639
Identifiers
- fda_app_no: ANDA208639
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2018-03-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE | 0.02MG;1MG | TABLET;ORAL |
1 product