FdaApplication
ANDA 206021
Identifiers
- fda_app_no: ANDA206021
Properties
| Property | Value |
|---|---|
| applicant_name | HEC PHARM USA INC |
| application_type | ANDA |
| approval_date | 2019-01-16 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PRASUGREL | PRASUGREL HYDROCHLORIDE | EQ 10MG BASE | TABLET;ORAL |
| PRASUGREL | PRASUGREL HYDROCHLORIDE | EQ 5MG BASE | TABLET;ORAL |
2 products