FdaApplication
ANDA 205421
Identifiers
- fda_app_no: ANDA205421
Properties
| Property | Value |
|---|---|
| applicant_name | ALEMBIC PHARMACEUTICALS LTD |
| application_type | ANDA |
| approval_date | 2019-07-01 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FEBUXOSTAT | FEBUXOSTAT | 40MG | TABLET;ORAL |
| FEBUXOSTAT | FEBUXOSTAT | 80MG | TABLET;ORAL |
2 products