FdaApplication
NDA 019816
Identifiers
- fda_app_no: NDA019816
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 1993-09-24 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ORUVAIL | KETOPROFEN | 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, EXTENDED RELEASE;ORAL |
| ORUVAIL | KETOPROFEN | 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, EXTENDED RELEASE;ORAL |
| ORUVAIL | KETOPROFEN | 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, EXTENDED RELEASE;ORAL |
3 products