FdaApplication
NDA 020169
Identifiers
- fda_app_no: NDA020169
Properties
| Property | Value |
|---|---|
| applicant_name | ADVANZ PHARMA (US) CORP |
| application_type | NDA |
| approval_date | 1996-09-19 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NILANDRON | NILUTAMIDE | 50MG | TABLET;ORAL |
| NILANDRON | NILUTAMIDE | 150MG | TABLET;ORAL |
2 products