FdaApplication
ANDA 074918
Identifiers
- fda_app_no: ANDA074918
Properties
| Property | Value |
|---|---|
| applicant_name | BARR LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1998-05-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALTREXONE HYDROCHLORIDE | NALTREXONE HYDROCHLORIDE | 50MG | TABLET;ORAL |
1 product