FdaApplication
NDA 021378
Identifiers
- fda_app_no: NDA021378
Properties
| Property | Value |
|---|---|
| applicant_name | FOREST LABORATORIES INC |
| application_type | NDA |
| approval_date | 2004-11-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| COMBUNOX | IBUPROFEN; OXYCODONE HYDROCHLORIDE | 400MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product