FdaApplication
NDA 020471
Identifiers
- fda_app_no: NDA020471
Properties
| Property | Value |
|---|---|
| applicant_name | CHIESI USA INC |
| application_type | NDA |
| approval_date | 1996-12-09 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZYFLO | ZILEUTON | 600MG | TABLET;ORAL |
| ZYFLO | ZILEUTON | 300MG | TABLET;ORAL |
2 products