FdaApplication
ANDA 210370
Identifiers
- fda_app_no: ANDA210370
Properties
| Property | Value |
|---|---|
| applicant_name | VISTAPHARM LLC |
| application_type | ANDA |
| approval_date | 2019-02-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MYCOPHENOLATE MOFETIL | MYCOPHENOLATE MOFETIL | 200MG/ML | FOR SUSPENSION;ORAL |
1 product