FdaApplication
NDA 022519
Identifiers
- fda_app_no: NDA022519
Properties
| Property | Value |
|---|---|
| applicant_name | HORIZON MEDICINES LLC |
| application_type | NDA |
| approval_date | 2011-04-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DUEXIS | FAMOTIDINE; IBUPROFEN | 26.6MG;800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product