FdaApplication
ANDA 076723
Identifiers
- fda_app_no: ANDA076723
Properties
| Property | Value |
|---|---|
| applicant_name | MPP PHARMA LLC |
| application_type | ANDA |
| approval_date | 2005-10-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE HYDROCHLORIDE | 8MG | TABLET;ORAL |
1 product