FdaApplication
ANDA 205239
Identifiers
- fda_app_no: ANDA205239
Properties
| Property | Value |
|---|---|
| applicant_name | EUGIA PHARMA SPECIALITIES LTD |
| application_type | ANDA |
| approval_date | 2016-02-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DANTROLENE SODIUM | DANTROLENE SODIUM | 20MG/VIAL | INJECTABLE;INJECTION |
1 product