FdaApplication
NDA 207999
Identifiers
- fda_app_no: NDA207999
Properties
| Property | Value |
|---|---|
| applicant_name | INTERCEPT PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2016-05-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OCALIVA | OBETICHOLIC ACID | 5MG | TABLET;ORAL |
| OCALIVA | OBETICHOLIC ACID | 10MG | TABLET;ORAL |
2 products