FdaApplication
ANDA 075082
Identifiers
- fda_app_no: ANDA075082
Properties
| Property | Value |
|---|---|
| applicant_name | VISTAPHARM LLC |
| application_type | ANDA |
| approval_date | 1998-03-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHADONE HYDROCHLORIDE | METHADONE HYDROCHLORIDE | 40MG | TABLET, FOR SUSPENSION;ORAL |
1 product