FdaApplication
NDA 215500
Identifiers
- fda_app_no: NDA215500
Properties
| Property | Value |
|---|---|
| applicant_name | USWM LLC |
| application_type | NDA |
| approval_date | 2023-12-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IWILFIN | EFLORNITHINE HYDROCHLORIDE | EQ 192MG BASE | TABLET;ORAL |
1 product