FdaApplication
NDA 204442
Identifiers
- fda_app_no: NDA204442
Properties
| Property | Value |
|---|---|
| applicant_name | REACX PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2016-05-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROBUPHINE | BUPRENORPHINE HYDROCHLORIDE | EQ 80MG BASE/IMPLANT | IMPLANT;IMPLANTATION |
1 product