FdaApplication
ANDA 070652
Identifiers
- fda_app_no: ANDA070652
Properties
| Property | Value |
|---|---|
| applicant_name | ABRAXIS PHARMACEUTICAL PRODUCTS |
| application_type | ANDA |
| approval_date | 1986-06-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLDOPATE HYDROCHLORIDE | METHYLDOPATE HYDROCHLORIDE | 50MG/ML | INJECTABLE;INJECTION |
1 product