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
- 47335-992_e4305694-0997-4791-a459-92e741b58130
- Product NDC
- 47335-992
- Form
- INJECTION, SOLUTION
- Composition / generic term
- magnesium sulfate heptahydrate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210801
- Source listing expiry
- 20271231
Source-listed ingredients
- MAGNESIUM SULFATE HEPTAHYDRATE — 40 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 24 POUCH in 1 CASE (47335-992-01) / 1 BAG in 1 POUCH / 50 mL in 1 BAG · 47335-992-01
- 24 POUCH in 1 CASE (47335-992-02) / 1 BAG in 1 POUCH / 100 mL in 1 BAG · 47335-992-02
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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