FdaApplication
ANDA 211374
Identifiers
- fda_app_no: ANDA211374
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2021-03-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MYCOPHENOLATE MOFETIL HYDROCHLORIDE | MYCOPHENOLATE MOFETIL HYDROCHLORIDE | 500MG/VIAL | INJECTABLE;INJECTION |
1 product