FdaApplication
ANDA 216739
Identifiers
- fda_app_no: ANDA216739
Properties
| Property | Value |
|---|---|
| applicant_name | APPCO PHARMA LLC |
| application_type | ANDA |
| approval_date | 2024-11-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CLOMIPHENE CITRATE | CLOMIPHENE CITRATE | 50MG | TABLET;ORAL |
1 product