FdaApplication
NDA 017604
Identifiers
- fda_app_no: NDA017604
Properties
| Property | Value |
|---|---|
| applicant_name | PHARMACO LLC |
| application_type | NDA |
| approval_date | 2009-07-21 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALFON | FENOPROFEN CALCIUM | EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
| NALFON | FENOPROFEN CALCIUM | EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
| NALFON | FENOPROFEN CALCIUM | EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
3 products