FdaApplication
ANDA 088519
Identifiers
- fda_app_no: ANDA088519
Properties
| Property | Value |
|---|---|
| applicant_name | SMITH AND NEPHEW SOLOPAK DIV SMITH AND NEPHEW |
| application_type | ANDA |
| approval_date | 1984-12-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PHENYTOIN SODIUM | PHENYTOIN SODIUM | 50MG/ML | INJECTABLE;INJECTION |
1 product