FdaApplication
NDA 216655
Identifiers
- fda_app_no: NDA216655
Properties
| Property | Value |
|---|---|
| applicant_name | XIAMEN LP PHARMACUETICAL CO LTD |
| application_type | NDA |
| approval_date | 2024-07-22 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OPIPZA | ARIPIPRAZOLE | 5MG | FILM;ORAL |
| OPIPZA | ARIPIPRAZOLE | 10MG | FILM;ORAL |
| OPIPZA | ARIPIPRAZOLE | 2MG | FILM;ORAL |
3 products