FdaApplication
ANDA 211043
Identifiers
- fda_app_no: ANDA211043
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2022-05-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZILEUTON | ZILEUTON | 600MG | TABLET, EXTENDED RELEASE;ORAL |
1 product