FdaApplication
ANDA 210201
Identifiers
- fda_app_no: ANDA210201
Properties
| Property | Value |
|---|---|
| applicant_name | ACQ PHARMA LLC |
| application_type | ANDA |
| approval_date | 2019-07-02 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MISOPROSTOL | MISOPROSTOL | 0.2MG | TABLET;ORAL |
| MISOPROSTOL | MISOPROSTOL | 0.1MG | TABLET;ORAL |
2 products