FdaApplication
ANDA 210959
Identifiers
- fda_app_no: ANDA210959
Properties
| Property | Value |
|---|---|
| applicant_name | LAURUS LABS LTD |
| application_type | ANDA |
| approval_date | 2019-01-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROXYCHLOROQUINE SULFATE | HYDROXYCHLOROQUINE SULFATE | 200MG | TABLET;ORAL |
1 product