FdaApplication
ANDA 208206
Identifiers
- fda_app_no: ANDA208206
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS |
| application_type | ANDA |
| approval_date | 2016-04-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RALOXIFENE HYDROCHLORIDE | RALOXIFENE HYDROCHLORIDE | 60MG | TABLET;ORAL |
1 product