FdaApplication
NDA 020584
Identifiers
- fda_app_no: NDA020584
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 1996-10-25 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LODINE XL | ETODOLAC | 600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
| LODINE XL | ETODOLAC | 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
| LODINE XL | ETODOLAC | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
3 products