FdaApplication
ANDA 089892
Identifiers
- fda_app_no: ANDA089892
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS MID ATLANTIC LLC |
| application_type | ANDA |
| approval_date | 1992-09-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PHENYTOIN | PHENYTOIN | 125MG/5ML | SUSPENSION;ORAL |
1 product