FdaApplication
ANDA 076129
Identifiers
- fda_app_no: ANDA076129
Properties
| Property | Value |
|---|---|
| applicant_name | AUROBINDO PHARMA USA INC |
| application_type | ANDA |
| approval_date | 2003-09-16 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NEFAZODONE HYDROCHLORIDE | NEFAZODONE HYDROCHLORIDE | 150MG | TABLET;ORAL |
| NEFAZODONE HYDROCHLORIDE | NEFAZODONE HYDROCHLORIDE | 250MG | TABLET;ORAL |
| NEFAZODONE HYDROCHLORIDE | NEFAZODONE HYDROCHLORIDE | 100MG | TABLET;ORAL |
| NEFAZODONE HYDROCHLORIDE | NEFAZODONE HYDROCHLORIDE | 200MG | TABLET;ORAL |
4 products