FdaApplication
NDA 209229
Identifiers
- fda_app_no: NDA209229
Properties
| Property | Value |
|---|---|
| applicant_name | BIOCORRX PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2018-05-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LUCEMYRA | LOFEXIDINE HYDROCHLORIDE | EQ 0.18MG BASE | TABLET;ORAL |
1 product