United States · FDA National Drug Code directory

MAGNESIUM SULFATE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
51662-1352_100d196c-c851-3cf7-e063-6294a90ad8c2
Product NDC
51662-1352
Form
INJECTION, SOLUTION
Composition / generic term
MAGNESIUM SULFATE
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Marketing category
NDA
Marketing start / end (source format)
20181221
Source listing expiry
20261231

Source-listed ingredients

  • MAGNESIUM SULFATE HEPTAHYDRATE — 40 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 50 mL in 1 BAG (51662-1352-1) · 51662-1352-1
  • 24 POUCH in 1 CASE (51662-1352-3) / 1 BAG in 1 POUCH (51662-1352-2) / 50 mL in 1 BAG · 51662-1352-3

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →