FdaApplication
ANDA 089900
Identifiers
- fda_app_no: ANDA089900
Properties
| Property | Value |
|---|---|
| applicant_name | WARNER CHILCOTT DIV WARNER LAMBERT CO |
| application_type | ANDA |
| approval_date | 1990-03-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PHENYTOIN SODIUM | PHENYTOIN SODIUM | 50MG/ML | INJECTABLE;INJECTION |
1 product