FdaApplication
ANDA 207567
Identifiers
- fda_app_no: ANDA207567
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC AN INDIRECT WHOLLY OWNED SUB OF TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2018-02-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TRIENTINE HYDROCHLORIDE | TRIENTINE HYDROCHLORIDE | 250MG | CAPSULE;ORAL |
1 product