FdaApplication
ANDA 077142
Identifiers
- fda_app_no: ANDA077142
Properties
| Property | Value |
|---|---|
| applicant_name | SPECGX LLC |
| application_type | ANDA |
| approval_date | 2005-07-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHADONE HYDROCHLORIDE | METHADONE HYDROCHLORIDE | 40MG | TABLET, FOR SUSPENSION;ORAL |
1 product