FdaApplication
ANDA 212797
Identifiers
- fda_app_no: ANDA212797
Properties
| Property | Value |
|---|---|
| applicant_name | XIAMEN LP PHARMACUETICAL CO LTD |
| application_type | ANDA |
| approval_date | 2021-06-11 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PRAMIPEXOLE DIHYDROCHLORIDE | PRAMIPEXOLE DIHYDROCHLORIDE | 0.75MG | TABLET, EXTENDED RELEASE;ORAL |
| PRAMIPEXOLE DIHYDROCHLORIDE | PRAMIPEXOLE DIHYDROCHLORIDE | 0.375MG | TABLET, EXTENDED RELEASE;ORAL |
2 products