FdaApplication
ANDA 210701
Identifiers
- fda_app_no: ANDA210701
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2022-05-19 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMBRISENTAN | AMBRISENTAN | 10MG | TABLET;ORAL |
| AMBRISENTAN | AMBRISENTAN | 5MG | TABLET;ORAL |
2 products