Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
| Pfizer Healthcare India Private Limited | Anakapalli, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 18, 2022 · 7 inspections, 1 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, intramuscular; intravenous; subcutaneous
- Strength
- 9 mg per 1 mL
- Approval
- NDA NDA018803
- On the market since
- Feb 28, 2005
- Package NDCs
0409-4888-010409-4888-020409-4888-030409-4888-060409-4888-100409-4888-120409-4888-200409-4888-500409-4888-90- Official label
- DailyMed (National Library of Medicine), updated Nov 6, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?