FdaApplication
ANDA 070136
Identifiers
- fda_app_no: ANDA070136
Properties
| Property | Value |
|---|---|
| applicant_name | SOLOPAK MEDICAL PRODUCTS INC |
| application_type | ANDA |
| approval_date | 1986-04-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 1MG/ML | INJECTABLE;INJECTION |
1 product