FdaApplication
ANDA 078302
Identifiers
- fda_app_no: ANDA078302
Properties
| Property | Value |
|---|---|
| applicant_name | OXFORD PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2007-12-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUSPIRONE HYDROCHLORIDE | BUSPIRONE HYDROCHLORIDE | 30MG | TABLET;ORAL |
1 product