FdaApplication
NDA 217159
Identifiers
- fda_app_no: NDA217159
Properties
| Property | Value |
|---|---|
| applicant_name | AYRMID PHARMA LTD |
| application_type | NDA |
| approval_date | 2023-09-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| APHEXDA | MOTIXAFORTIDE ACETATE | EQ 62MG BASE/VIAL | POWDER;SUBCUTANEOUS |
1 product