FdaApplication
ANDA 207355
Identifiers
- fda_app_no: ANDA207355
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS LABORATORIES FL INC |
| application_type | ANDA |
| approval_date | 2022-11-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| POSACONAZOLE | POSACONAZOLE | 100MG | TABLET, DELAYED RELEASE;ORAL |
1 product