FdaApplication
ANDA 070031
Identifiers
- fda_app_no: ANDA070031
Properties
| Property | Value |
|---|---|
| applicant_name | ABRAXIS PHARMACEUTICAL PRODUCTS |
| application_type | ANDA |
| approval_date | 1985-01-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM NITROPRUSSIDE | SODIUM NITROPRUSSIDE | 50MG/VIAL | INJECTABLE;INJECTION |
1 product