FdaApplication
ANDA 213815
Identifiers
- fda_app_no: ANDA213815
Properties
| Property | Value |
|---|---|
| applicant_name | APPCO PHARMA LLC |
| application_type | ANDA |
| approval_date | 2020-10-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RAMELTEON | RAMELTEON | 8MG | TABLET;ORAL |
1 product