FdaApplication
ANDA 213331
Identifiers
- fda_app_no: ANDA213331
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2026-06-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| POSACONAZOLE | POSACONAZOLE | 100MG | TABLET, DELAYED RELEASE;ORAL |
1 product