FdaApplication
ANDA 206384
Identifiers
- fda_app_no: ANDA206384
Properties
| Property | Value |
|---|---|
| applicant_name | SCIEGEN PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 2016-10-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RALOXIFENE HYDROCHLORIDE | RALOXIFENE HYDROCHLORIDE | 60MG | TABLET;ORAL |
1 product