FdaApplication
NDA 208085
Identifiers
- fda_app_no: NDA208085
Properties
| Property | Value |
|---|---|
| applicant_name | ECI PHARMACEUTICALS LLC |
| application_type | NDA |
| approval_date | 2018-04-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| XTRELUS | GUAIFENESIN; HYDROCODONE BITARTRATE | 400MG;5MG | TABLET;ORAL |
1 product