FdaApplication
NDA 213150
Identifiers
- fda_app_no: NDA213150
Properties
| Property | Value |
|---|---|
| applicant_name | TOLMAR INTERNATIONAL LTD |
| application_type | NDA |
| approval_date | 2020-05-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FENSOLVI KIT | LEUPROLIDE ACETATE | 45MG | POWDER;SUBCUTANEOUS |
1 product