FdaApplication
ANDA 207259
Identifiers
- fda_app_no: ANDA207259
Properties
| Property | Value |
|---|---|
| applicant_name | XIROMED LLC |
| application_type | ANDA |
| approval_date | 2016-12-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE | 0.005MG;1MG | TABLET;ORAL |
1 product