FdaApplication
ANDA 204762
Identifiers
- fda_app_no: ANDA204762
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2017-06-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DANTROLENE SODIUM | DANTROLENE SODIUM | 20MG/VIAL | INJECTABLE;INJECTION |
1 product