FdaApplication
ANDA 075434
Identifiers
- fda_app_no: ANDA075434
Properties
| Property | Value |
|---|---|
| applicant_name | NOVITIUM PHARMA LLC |
| application_type | ANDA |
| approval_date | 2000-03-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALTREXONE HYDROCHLORIDE | NALTREXONE HYDROCHLORIDE | 50MG | TABLET;ORAL |
1 product