FdaApplication
ANDA 202138
Identifiers
- fda_app_no: ANDA202138
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2019-03-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| KEMEYA | DROSPIRENONE; ETHINYL ESTRADIOL | 3MG;0.03MG | TABLET;ORAL-28 |
1 product