FdaApplication
ANDA 088711
Identifiers
- fda_app_no: ANDA088711
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1984-12-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PHENYTEX | PHENYTOIN SODIUM | 100MG EXTENDED | CAPSULE;ORAL |
1 product