FdaApplication
ANDA 078394
Identifiers
- fda_app_no: ANDA078394
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 2007-11-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE HYDROCHLORIDE AND IBUPROFEN | IBUPROFEN; OXYCODONE HYDROCHLORIDE | 400MG;5MG | TABLET;ORAL |
1 product