FdaApplication
NDA 020450
Identifiers
- fda_app_no: NDA020450
Properties
| Property | Value |
|---|---|
| applicant_name | PARKE DAVIS DIV WARNER LAMBERT CO |
| application_type | NDA |
| approval_date | 1996-08-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEREBYX | FOSPHENYTOIN SODIUM | EQ 50MG PHENYTOIN NA/ML | INJECTABLE;INJECTION |
1 product