FdaApplication
ANDA 209787
Identifiers
- fda_app_no: ANDA209787
Properties
| Property | Value |
|---|---|
| applicant_name | LOTUS PHARMACEUTICAL CO LTD NANTOU PLANT |
| application_type | ANDA |
| approval_date | 2021-04-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHOTREXATE SODIUM | METHOTREXATE SODIUM | EQ 2.5MG BASE | TABLET;ORAL |
1 product