FdaApplication
ANDA 078769
Identifiers
- fda_app_no: ANDA078769
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS ELIZABETH LLC |
| application_type | ANDA |
| approval_date | 2008-01-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE HYDROCHLORIDE AND IBUPROFEN | IBUPROFEN; OXYCODONE HYDROCHLORIDE | 400MG;5MG | TABLET;ORAL |
1 product