NDC 51754-1029
Nipride Rtu 0.2 mg per 1 mL injection, solution
On the label: Exela Pharma Sciences, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Exela Pharma Sciences, LLC. | Lenoir, NC, United States | Makes it | Serious problems, FDA actionNov 15, 2024 · 12 inspections, 1 with FDA action |
Product details
- Generic drug
- Nitroprusside: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 0.2 mg per 1 mL
- Approval
- NDA NDA209387
- On the market since
- Jul 20, 2018
- Package NDCs
51754-1029-1- Official label
- DailyMed (National Library of Medicine), updated Jul 20, 2018
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