FdaApplication
ANDA 209532
Identifiers
- fda_app_no: ANDA209532
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2022-09-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GEFITINIB | GEFITINIB | 250MG | TABLET;ORAL |
1 product