FdaApplication
ANDA 078378
Identifiers
- fda_app_no: ANDA078378
Properties
| Property | Value |
|---|---|
| applicant_name | USWM LLC |
| application_type | ANDA |
| approval_date | 2007-07-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| REVONTO | DANTROLENE SODIUM | 20MG/VIAL | INJECTABLE;INJECTION |
1 product