FdaApplication
ANDA 075274
Identifiers
- fda_app_no: ANDA075274
Properties
| Property | Value |
|---|---|
| applicant_name | ELITE LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1999-05-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALTREXONE HYDROCHLORIDE | NALTREXONE HYDROCHLORIDE | 50MG | TABLET;ORAL |
1 product