FdaApplication
ANDA 205630
Identifiers
- fda_app_no: ANDA205630
Properties
| Property | Value |
|---|---|
| applicant_name | LUPIN LTD |
| application_type | ANDA |
| approval_date | 2016-10-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NORGESTIMATE AND ETHINYL ESTRADIOL | ETHINYL ESTRADIOL; NORGESTIMATE | 0.035MG;0.25MG | TABLET;ORAL-28 |
1 product