FdaApplication
NDA 214511
Identifiers
- fda_app_no: NDA214511
Properties
| Property | Value |
|---|---|
| applicant_name | LUMICELL INC |
| application_type | NDA |
| approval_date | 2024-04-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LUMISIGHT | PEGULICIANINE ACETATE | EQ 39MG BASE/VIAL | POWDER;INTRAVENOUS |
1 product