FdaApplication
ANDA 070800
Identifiers
- fda_app_no: ANDA070800
Properties
| Property | Value |
|---|---|
| applicant_name | SOLOPAK MEDICAL PRODUCTS INC |
| application_type | ANDA |
| approval_date | 1987-12-14 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALOPERIDOL | HALOPERIDOL LACTATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION |
1 product