NDC 51662-1352
Magnesium Sulfate 40 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hospira, Inc.'s NDC 0409-6729.
Where the pills inside were 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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Oct 3, 2018 · Class II · Pfizer Inc.
Correct Labeled Product Mispack: confirmed report involving a single unit of properly labeled Heparin in 0.45% Sodium Chloride for Injection (NDC 0409-7651-03, Lot 87903FW) that was found inside a case of Magnesium Sulfate in Water for Injection.
Lots: Lot: 87904FW, Exp. 1MAR2020 - 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 mg per 1 mL
- Approval
- NDA NDA020309
- On the market since
- Dec 21, 2018
- Package NDCs
51662-1352-151662-1352-251662-1352-3- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2024
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