FdaApplication
NDA 207931
Identifiers
- fda_app_no: NDA207931
Properties
| Property | Value |
|---|---|
| applicant_name | ABBVIE INC |
| application_type | NDA |
| approval_date | 2015-07-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TECHNIVIE | OMBITASVIR; PARITAPREVIR; RITONAVIR | 12.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product