FdaApplication
ANDA 206969
Identifiers
- fda_app_no: ANDA206969
Properties
| Property | Value |
|---|---|
| applicant_name | GLENMARK PHARMACEUTICALS LTD |
| application_type | ANDA |
| approval_date | 2016-01-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE | 0.02MG;1MG | TABLET;ORAL-21 |
1 product