NDC 51662-1372-01 - MAGNESIUM SULFATE

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 51662-1372
Requested NDC: 51662-1372-01
Package NDCs from labels: 51662-1372-1, 51662-1372-01
Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Effective date: 2022-12-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
MAGNESIUM SULFATE - HF Acquisition Co LLC, DBA HealthFirst	HF Acquisition Co LLC, DBA HealthFirst	2022-12-10	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51662-1372-1	MAGNESIUM SULFATE	20 mL in 1 VIAL, SINGLE-DOSE	INJECTION, SOLUTION	20		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51662-1372	MAGNESIUM SULFATE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST]	3	Current NDC, Legacy NDC, 1 package rows	20221211_94e9a33f-39c4-4bc5-e053-2a95a90a43ac.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 6 of 6 · 104 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Magnesium Sulfate	MAGNESIUM SULFATE HEPTAHYDRATE	Medical Purchasing Solutions, LLC	b6352fbd-d3ee-2d3a-e053-2a95a90a747d	2020-12-11	Warnings, Adverse reactions	Exact identifier application number: NDA019316 unii: SK47B8698T
Magnesium Sulfate	MAGNESIUM SULFATE HEPTAHYDRATE	Sagent Pharmaceuticals	a607796c-6676-4d0a-8108-8708fe6769ed	2020-11-16	Warnings, Adverse reactions	Exact identifier unii: SK47B8698T
MAGNESIUM SULFATE	MAGNESIUM SULFATE HEPTAHYDRATE	Gland Pharma Limited	a9e706ac-9c5f-4b14-b277-53dee195ffc6	2020-07-14	Warnings, Adverse reactions	Exact identifier unii: SK47B8698T
TIS-U-SOL	SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE	Baxter Healthcare Corporation	9da4121f-d62d-4da4-8dfb-0494da16015f	2014-02-21		Exact identifier unii: SK47B8698T

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.