FdaApplication
ANDA 040731
Identifiers
- fda_app_no: ANDA040731
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2008-06-30 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EXTENDED PHENYTOIN SODIUM | PHENYTOIN SODIUM | 200MG EXTENDED | CAPSULE;ORAL |
| EXTENDED PHENYTOIN SODIUM | PHENYTOIN SODIUM | 300MG EXTENDED | CAPSULE;ORAL |
2 products