NDC 17271-701
Sodium chloride 9 mg per 1 mL injection, solution
On the label: Becton Dickinson and Company.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi Deutschland GmbH | Friedberg, Germany | Makes it, makes the active ingredient and tests it | Problems found, fixed voluntarilyDec 21, 2023 · 4 inspections |
| Fresenius Kabi USA, LLC | Wilson, NC, United States | Makes it and tests it | Problems found, fixed voluntarilyFeb 13, 2026 · 5 inspections |
| Fresenius Medical Care North America | Ogden, UT, United States | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionMar 6, 2026 · 8 inspections, 1 with FDA action |
| HP Halden Pharma AS | Halden, Norway | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 10, 2023 · 7 inspections |
Recalls
- Mar 11, 2026 · Class II · Fresenius Kabi USA, LLC
Lack of Assurance of Sterility
Lots: Batch# 6402428, Exp Date: 10/31/2026; Batch# 6402481, 6402482, Exp Date: 11/30/2026. - Mar 11, 2026 · Class II · Fresenius Kabi USA, LLC
Lack of Assurance of Sterility
Lots: Batch# 6402153, Exp Date: 11/30/2026; Batch# 6402297, 6402298, Exp Date: 01/31/2027; Batch# 6402377, 6402378, 6402379, Exp Date: 02/28/2027; Batch # 6402429, 6402430, 6402431, 6402432, 6402433, Exp Date: 03/31/2027; Batch# 6402434, Exp Date: 04/30/2027; Batch# 6402512, Exp Date: 05/2027; Batch# 640… - Mar 11, 2026 · Class II · Fresenius Kabi USA, LLC
Lack of Assurance of Sterility
Lots: Batch# 6402290, 6402291, Exp Date: 01/31/2028; Batch# 6402411, Exp Date: 02/29/2028; Batch# 6402412, 6402419, 6402424, 6402425, 6402426, 6402427, Exp Date: 03/31/2028; Batch# 6402479, 6402480, 6402517, 6402571, Exp Date: 05/31/2028; Batch# 6402518, Exp Date: 06/30/2028. - Mar 11, 2026 · Class II · Fresenius Kabi USA, LLC
Lack of Assurance of Sterility
Lots: Batch# 24EU10010, Exp Date: 05/31/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sodium Cation: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 9 mg per 1 mL
- Approval
- ANDA ANDA207310
- On the market since
- Sep 19, 2017
- Package NDCs
17271-701-0217271-701-0317271-701-0517271-701-0617271-701-07- Official label
- DailyMed (National Library of Medicine), updated May 21, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?