FdaApplication
ANDA 201661
Identifiers
- fda_app_no: ANDA201661
Properties
| Property | Value |
|---|---|
| applicant_name | LUPIN LTD |
| application_type | ANDA |
| approval_date | 2014-05-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NIKKI | DROSPIRENONE; ETHINYL ESTRADIOL | 3MG;0.02MG | TABLET;ORAL |
1 product