FdaApplication
ANDA 071517
Identifiers
- fda_app_no: ANDA071517
Properties
| Property | Value |
|---|---|
| applicant_name | SUPERPHARM CORP |
| application_type | ANDA |
| approval_date | 1988-06-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 40MG | TABLET;ORAL |
1 product