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
- 51662-1390_ed27a836-95ca-a8a9-e053-2a95a90a6f0d
- Product NDC
- 51662-1390
- Form
- INJECTION, SOLUTION
- Composition / generic term
- MAGNESIUM SULFATE
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Marketing category
- NDA
- Marketing start / end (source format)
- 20191007
- Source listing expiry
- 20261231
Source-listed ingredients
- MAGNESIUM SULFATE HEPTAHYDRATE — 500 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 mL in 1 VIAL, SINGLE-DOSE (51662-1390-1) · 51662-1390-1
- 25 POUCH in 1 CASE (51662-1390-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1390-2) / 2 mL in 1 VIAL, SINGLE-DOSE · 51662-1390-3
Source and coverage
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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.
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