# SUTAB

NDC: 24338-201
Generic name: sodium sulfate, magnesium sulfate, and potassium chloride
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260401

FDA application: NDA213135

## Active ingredients

- MAGNESIUM SULFATE ANHYDROUS: 2.7 g/1
- POTASSIUM CHLORIDE: 2.25 g/1
- SODIUM SULFATE: 17.75 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24338-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24338-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c020e973-dccf-4862-999e-17db6209a48a