FdaApplication
ANDA 075388
Identifiers
- fda_app_no: ANDA075388
Properties
| Property | Value |
|---|---|
| applicant_name | OXFORD PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2002-05-09 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUSPIRONE HYDROCHLORIDE | BUSPIRONE HYDROCHLORIDE | 10MG | TABLET;ORAL |
| BUSPIRONE HYDROCHLORIDE | BUSPIRONE HYDROCHLORIDE | 5MG | TABLET;ORAL |
| BUSPIRONE HYDROCHLORIDE | BUSPIRONE HYDROCHLORIDE | 15MG | TABLET;ORAL |
3 products