# SUPREP Bowel Prep

NDC: 24338-177
Generic name: sodium sulfate, potassium sulfate, magnesium sulfate
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION, CONCENTRATE
Routes: ORAL
Marketing started: 20260401

FDA application: NDA022372

## Active ingredients

- MAGNESIUM SULFATE, UNSPECIFIED FORM: 1.2 g/133.1mL
- POTASSIUM SULFATE: 2.35 g/133.1mL
- SODIUM SULFATE: 13.13 g/133.1mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24338-177"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24338-177
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=50f23abd-6a66-44cb-960e-d43c16a5ae5f