FdaApplication
ANDA 088917
Identifiers
- fda_app_no: ANDA088917
Properties
| Property | Value |
|---|---|
| applicant_name | USL PHARMA INC |
| application_type | ANDA |
| approval_date | 1985-07-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PHENTERMINE HYDROCHLORIDE | PHENTERMINE HYDROCHLORIDE | 37.5MG | TABLET;ORAL |
1 product