FdaApplication
ANDA 207139
Identifiers
- fda_app_no: ANDA207139
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS LABORATORIES FL INC |
| application_type | ANDA |
| approval_date | 2017-06-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PAROXETINE MESYLATE | PAROXETINE MESYLATE | EQ 7.5MG BASE | CAPSULE;ORAL |
1 product