FdaApplication
NDA 211672
Identifiers
- fda_app_no: NDA211672
Properties
| Property | Value |
|---|---|
| applicant_name | HONG KONG KING FRIEND INDUSTRIAL CO LTD |
| application_type | NDA |
| approval_date | 2019-08-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| XENLETA | LEFAMULIN ACETATE | EQ 600MG BASE | TABLET;ORAL |
1 product