FdaApplication
ANDA 072192
Identifiers
- fda_app_no: ANDA072192
Properties
| Property | Value |
|---|---|
| applicant_name | OXFORD PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 1989-02-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TRAZODONE HYDROCHLORIDE | TRAZODONE HYDROCHLORIDE | 50MG | TABLET;ORAL |
1 product