FdaApplication
ANDA 216390
Identifiers
- fda_app_no: ANDA216390
Properties
| Property | Value |
|---|---|
| applicant_name | ONESOURCE SPECIALTY PTE LTD |
| application_type | ANDA |
| approval_date | 2022-12-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MYCOPHENOLATE MOFETIL HYDROCHLORIDE | MYCOPHENOLATE MOFETIL HYDROCHLORIDE | 500MG/VIAL | INJECTABLE;INJECTION |
1 product