FdaApplication
ANDA 217695
Identifiers
- fda_app_no: ANDA217695
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2023-08-23 |
Products (7)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEXAMETHASONE | DEXAMETHASONE | 1.5MG | TABLET;ORAL |
| DEXAMETHASONE | DEXAMETHASONE | 0.5MG | TABLET;ORAL |
| DEXAMETHASONE | DEXAMETHASONE | 0.75MG | TABLET;ORAL |
| DEXAMETHASONE | DEXAMETHASONE | 1MG | TABLET;ORAL |
| DEXAMETHASONE | DEXAMETHASONE | 4MG | TABLET;ORAL |
| DEXAMETHASONE | DEXAMETHASONE | 2MG | TABLET;ORAL |
| DEXAMETHASONE | DEXAMETHASONE | 6MG | TABLET;ORAL |
7 products