NDC 51754-0103
Cupric Chloride 0.4 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, tests it and packages it | Serious problems, FDA actionNov 15, 2024 · 12 inspections, 1 with FDA action |
Product details
- Generic drug
- Cupric Cation: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 0.4 mg per 1 mL
- Approval
- ANDA ANDA212071
- On the market since
- Feb 1, 2023
- Package NDCs
51754-0103-351754-0103-4- Official label
- DailyMed (National Library of Medicine), updated May 16, 2019
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