FdaApplication
ANDA 070121
Identifiers
- fda_app_no: ANDA070121
Properties
| Property | Value |
|---|---|
| applicant_name | SCHERING CORP SUB SCHERING PLOUGH CORP |
| application_type | ANDA |
| approval_date | 1985-08-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 20MG | TABLET;ORAL |
1 product