FdaApplication
ANDA 210369
Identifiers
- fda_app_no: ANDA210369
Properties
| Property | Value |
|---|---|
| applicant_name | GLENMARK PHARMACEUTICALS LTD |
| application_type | ANDA |
| approval_date | 2017-12-26 |
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