FdaApplication
NDA 018922
Identifiers
- fda_app_no: NDA018922
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 1991-01-31 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LODINE | ETODOLAC | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| LODINE | ETODOLAC | 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
| LODINE | ETODOLAC | 300MG | CAPSULE;ORAL |
| LODINE | ETODOLAC | 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
4 products