FdaApplication
NDA 018754
Identifiers
- fda_app_no: NDA018754
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH AYERST LABORATORIES |
| application_type | NDA |
| approval_date | 1986-01-09 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ORUDIS | KETOPROFEN | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
| ORUDIS | KETOPROFEN | 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
| ORUDIS | KETOPROFEN | 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
3 products