FdaApplication
ANDA 209632
Identifiers
- fda_app_no: ANDA209632
Properties
| Property | Value |
|---|---|
| applicant_name | AUROBINDO PHARMA LTD |
| application_type | ANDA |
| approval_date | 2018-02-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LO-ZUMANDIMINE | DROSPIRENONE; ETHINYL ESTRADIOL | 3MG;0.02MG | TABLET;ORAL |
1 product