FdaApplication
ANDA 211436
Identifiers
- fda_app_no: ANDA211436
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2020-08-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MIFEPRISTONE | MIFEPRISTONE | 300MG | TABLET;ORAL |
1 product