United States · FDA National Drug Code directory
SUTAB
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
- 24338-201_c020e973-dccf-4862-999e-17db6209a48a
- Product NDC
- 24338-201
- Form
- TABLET
- Composition / generic term
- sodium sulfate, magnesium sulfate, and potassium chloride
- Labeler
- Azurity Pharmaceuticals, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20260401
- Source listing expiry
- 20271231
Source-listed ingredients
- SODIUM SULFATE — 17.75 g/1
- MAGNESIUM SULFATE ANHYDROUS — 2.7 g/1
- POTASSIUM CHLORIDE — 2.25 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE, PLASTIC in 1 KIT (24338-201-01) / 12 TABLET in 1 BOTTLE, PLASTIC · 24338-201-01
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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