FdaApplication
NDA 213225
Identifiers
- fda_app_no: NDA213225
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARM |
| application_type | NDA |
| approval_date | 2026-08-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VOBRIG | LEUPROLIDE ACETATE | 28MG/2.8ML (10MG/ML) | SOLUTION;SUBCUTANEOUS |
1 product