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
- 31722-394_36bf495e-3966-8317-e063-6294a90a055f
- Product NDC
- 31722-394
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Magnesium sulfate heptahydrate
- Labeler
- Camber Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250528
- Source listing expiry
- 20261231
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 CARTON (31722-394-32) / 2 mL in 1 VIAL, SINGLE-DOSE (31722-394-31) · 31722-394-32
- 25 VIAL, SINGLE-DOSE in 1 CARTON (31722-394-33) / 10 mL in 1 VIAL, SINGLE-DOSE (31722-394-10) · 31722-394-33
- 25 VIAL, SINGLE-DOSE in 1 CARTON (31722-394-34) / 20 mL in 1 VIAL, SINGLE-DOSE (31722-394-20) · 31722-394-34
- 25 VIAL, SINGLE-DOSE in 1 CARTON (31722-394-35) / 50 mL in 1 VIAL, SINGLE-DOSE (31722-394-50) · 31722-394-35
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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