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
- 70518-4375_59ca0262-cae8-b088-e063-6294a90a3166
- Product NDC
- 70518-4375
- Form
- INJECTION, SOLUTION
- Composition / generic term
- MAGNESIUM SULFATE HEPTAHYDRATE
- Labeler
- REMEDYREPACK INC.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20250628
- Source listing expiry
- 20271231
Source-listed ingredients
- MAGNESIUM SULFATE HEPTAHYDRATE — 500 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 TRAY (70518-4375-0) / 10 mL in 1 VIAL, SINGLE-DOSE (70518-4375-1) · 70518-4375-0
- 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4375-2) / 2 mL in 1 VIAL, SINGLE-DOSE (70518-4375-3) · 70518-4375-2
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 →