Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | McPherson, KS, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
Recalls
- Jun 27, 2013 · Class II · Hospira Inc.
Presence of Particulate Matter: Confirmed customer report of visible particulate in the form of an orange or rust colored ring embedded in between the plastic layers of the plastic vial.
Lots: Lot #: 15-058-DK*, Exp 1MAR2014; note the * may be followed by 01
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Chloride Ion: every company that makes it
- Form
- injection, solution
- Strength
- 9 mg per 1 mL
- Approval
- NDA NDA018803
- On the market since
- Feb 28, 2005
- Package NDCs
0409-1918-320409-1918-330409-1918-350409-1918-420409-1918-430409-1918-45- Official label
- DailyMed (National Library of Medicine), updated Nov 6, 2024
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