FdaApplication
ANDA 208305
Identifiers
- fda_app_no: ANDA208305
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 2018-03-30 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHADONE HYDROCHLORIDE | METHADONE HYDROCHLORIDE | 10MG | TABLET;ORAL |
| METHADONE HYDROCHLORIDE | METHADONE HYDROCHLORIDE | 5MG | TABLET;ORAL |
2 products