FdaApplication
NDA 020429
Identifiers
- fda_app_no: NDA020429
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH CONSUMER HEALTHCARE |
| application_type | NDA |
| approval_date | 1995-10-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ORUDIS KT | KETOPROFEN | 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product