United States · FDA National Drug Code directory
Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit
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
- 51672-4170_494f52da-8ae6-6ec4-e063-6294a90a73a6
- Product NDC
- 51672-4170
- Form
- SOLUTION
- Composition / generic term
- sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240327
- Source listing expiry
- 20271231
Source-listed ingredients
- SODIUM SULFATE ANHYDROUS — 17.5 g/177mL
- POTASSIUM SULFATE — 3.13 g/177mL
- MAGNESIUM SULFATE, UNSPECIFIED FORM — 1.6 g/177mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE in 1 CARTON (51672-4170-5) / 177 mL in 1 BOTTLE · 51672-4170-5
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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