FdaApplication
NDA 210557
Identifiers
- fda_app_no: NDA210557
Properties
| Property | Value |
|---|---|
| applicant_name | COSETTE PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2019-06-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VYLEESI (AUTOINJECTOR) | BREMELANOTIDE ACETATE | EQ 1.75MG BASE/0.3ML (EQ 1.75MG BASE/0.3 ML) | SOLUTION;SUBCUTANEOUS |
1 product