FdaApplication
ANDA 200825
Identifiers
- fda_app_no: ANDA200825
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 2015-01-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RALOXIFENE HYDROCHLORIDE | RALOXIFENE HYDROCHLORIDE | 60MG | TABLET;ORAL |
1 product