FdaApplication
NDA 020687
Identifiers
- fda_app_no: NDA020687
Properties
| Property | Value |
|---|---|
| applicant_name | DANCO LABORATORIES LLC |
| application_type | NDA |
| approval_date | 2000-09-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MIFEPREX | MIFEPRISTONE | 200MG | TABLET;ORAL |
1 product