Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceuticals Injectables Inc. | Baltimore, MD, United States | Makes it | Problems found, fixed voluntarilyAug 10, 2023 · 12 inspections, 1 with FDA action |
| Curia New York, Inc. | Rensselaer, NY, United States | Makes the active ingredient | Serious problems, FDA actionFeb 5, 2026 · 8 inspections, 1 with FDA action |
| Siegfried Grafton, Inc. | Grafton, WI, United States | Makes the active ingredient | Problems found, fixed voluntarilyAug 21, 2026 · 7 inspections |
| Sterling Wisconsin, LLC | Germantown, WI, United States | Makes the active ingredient | No problems foundMar 12, 2024 · 6 inspections |
Product details
- Generic drug
- Nitrite Ion and Thiosulfate Ion: every company that makes it
- Form
- kit
- Strength
- 30 mg per 1 mL / 250 mg per 1 mL
- Approval
- NDA NDA201444
- On the market since
- Jan 14, 2011
- Package NDCs
60267-311-1060267-705-5060267-812-00- Official label
- DailyMed (National Library of Medicine), updated Oct 6, 2025
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