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MAGNESIUM SULFATE

NDC 51662-1372, MAGNESIUM SULFATE, injection, solution, from HF Acquisition Co LLC, DBA HealthFirst.

Product NDC
51662-1372
Status
Listed
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA019316
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1372 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MAGNESIUM SULFATE HEPTAHYDRATE500 mg/mL

Pharmacologic classes

Calculi Dissolution Agent [EPC]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Package NDCNDC-11Package
51662-1372-15166213720120 mL in 1 VIAL, SINGLE-DOSE (51662-1372-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/94e9a33f-39c4-4bc5-e053-2a95a90a43ac

Use it

Look up 51662-1372 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1372 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51662-1372. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.