FdaApplication
ANDA 213522
Identifiers
- fda_app_no: ANDA213522
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2025-03-14 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ELUXADOLINE | ELUXADOLINE | 75MG | TABLET;ORAL |
| ELUXADOLINE | ELUXADOLINE | 100MG | TABLET;ORAL |
2 products