FdaApplication
NDA 204958
Identifiers
- fda_app_no: NDA204958
Properties
| Property | Value |
|---|---|
| applicant_name | CHIESI USA INC |
| application_type | NDA |
| approval_date | 2015-06-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| KENGREAL | CANGRELOR | 50MG/VIAL | POWDER;INTRAVENOUS |
1 product