FdaApplication
NDA 218590
Identifiers
- fda_app_no: NDA218590
Properties
| Property | Value |
|---|---|
| applicant_name | KNOA PHARMA LLC |
| application_type | NDA |
| approval_date | 2024-08-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZURNAI (AUTOINJECTOR) | NALMEFENE HYDROCHLORIDE | EQ 1.5MG BASE/0.5ML (EQ 1.5MG BASE/0.5ML) | SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS |
1 product