NDC 87333-001
Cardiolite 1 mg per 1 mL injection, powder, lyophilized, for solution
On the label: Shine Spect USA, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Jubilant HollisterStier LLC | Spokane, WA, United States | Makes it and tests it | No problems foundMar 5, 2021 · 13 inspections, 1 with FDA action |
| Shine Spect USA,LLC | North Billerica, MA, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 10, 2026 · 1 inspection |
Product details
- Generic drug
- Tetrakis(2-Methoxyisobutylisocyanide)copper(i) Tetrafluoroborate: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 1 mg per 1 mL
- Approval
- NDA NDA019785
- On the market since
- Sep 10, 2026
- Package NDCs
87333-001-2087333-001-55- Official label
- DailyMed (National Library of Medicine), updated Sep 10, 2026
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