FdaApplication
ANDA 200151
Identifiers
- fda_app_no: ANDA200151
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2014-02-03 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SELFEMRA | FLUOXETINE HYDROCHLORIDE | EQ 10MG BASE | TABLET;ORAL |
| SELFEMRA | FLUOXETINE HYDROCHLORIDE | EQ 15MG BASE | TABLET;ORAL |
| SELFEMRA | FLUOXETINE HYDROCHLORIDE | EQ 20MG BASE | TABLET;ORAL |
3 products