FdaApplication
ANDA 211972
Identifiers
- fda_app_no: ANDA211972
Properties
| Property | Value |
|---|---|
| applicant_name | LUPIN LTD |
| application_type | ANDA |
| approval_date | 2019-11-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZILEUTON | ZILEUTON | 600MG | TABLET, EXTENDED RELEASE;ORAL |
1 product