FdaApplication
ANDA 213239
Identifiers
- fda_app_no: ANDA213239
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | ANDA |
| approval_date | 2021-03-29 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEFERIPRONE | DEFERIPRONE | 500MG | TABLET;ORAL |
| DEFERIPRONE | DEFERIPRONE | 1GM | TABLET;ORAL |
2 products