FdaApplication
ANDA 071555
Identifiers
- fda_app_no: ANDA071555
Properties
| Property | Value |
|---|---|
| applicant_name | ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV |
| application_type | ANDA |
| approval_date | 1987-11-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NITROPRESS | SODIUM NITROPRUSSIDE | 50MG/VIAL | INJECTABLE;INJECTION |
1 product