FdaApplication
ANDA 076004
Identifiers
- fda_app_no: ANDA076004
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2002-12-03 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ETODOLAC | ETODOLAC | 500MG | TABLET;ORAL |
| ETODOLAC | ETODOLAC | 400MG | TABLET;ORAL |
2 products