FdaApplication
ANDA 078316
Identifiers
- fda_app_no: ANDA078316
Properties
| Property | Value |
|---|---|
| applicant_name | BARR LABORATORIES INC |
| application_type | ANDA |
| approval_date | 2007-11-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE HYDROCHLORIDE AND IBUPROFEN | IBUPROFEN; OXYCODONE HYDROCHLORIDE | 400MG;5MG | TABLET;ORAL |
1 product