NDC 0409-3164
Magnesium Sulfate in Water 40 g per 1000 mL injection, solution
On the label: Hospira, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hospira, Inc. names for other drugs.
Recalls
- Jan 5, 2016 · Class I · Hospira Inc.
Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wrong barcode which scans in as heparin sodium.
Lots: Lot: 53-113-JT, Exp 1NOV2016 - Apr 5, 2012 · Class III · Hospira, Inc.
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
Lots: Lot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Magnesium Cation: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 40 g per 1000 mL
- Approval
- NDA NDA020309
- On the market since
- Jun 19, 2023
- Package NDCs
0409-3164-010409-3164-12- Official label
- DailyMed (National Library of Medicine), updated Aug 24, 2026
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