Orange Book product
SODIUM NITROPRUSSIDE 50MG/VIAL
Orange Book ANDA 070031 · ABRAXIS PHARMACEUTICAL PRODUCTS · Discontinued
Key facts
| Proprietary name | SODIUM NITROPRUSSIDE |
|---|---|
| Active ingredients | SODIUM NITROPRUSSIDE |
| Strength | 50MG/VIAL |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Application | ANDA070031 |
| Applicant holder | ABRAXIS PHARMACEUTICAL PRODUCTS |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Jan 17, 1985 |
At a glance
- None Marketed products with the same ingredient, strength and form
- 1–9 Products in this application
- No Reference listed drug
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Orange Book products
The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.