NDC 24338-175 – SUPREP Bowel Prep

Sodium Sulfate 17.5 g/mL; Potassium Sulfate 3.13 g/mL; Magnesium Sulfate, Unspecified Form 1.6 g/mL · Solution, Concentrate · Oral

Human Prescription Drug

Product NDC24338-175

Product details

Brand name
SUPREP Bowel Prep
Generic name
Sodium sulfate, potassium sulfate, magnesium sulfate
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
Solution, Concentrate
Route
Oral
Marketing category
NDA · NDA022372
Marketed since
April 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Calculi Dissolution Agent; Osmotic Laxative; Osmotic Laxative; Osmotic Laxative; Potassium Salt

Active ingredients

Uses, dosage, side effects and warnings for SUPREP Bowel Prep →

Package NDC codes (1)

Package NDCDescriptionSince
24338-175-012 BOTTLE, PLASTIC in 1 CARTON (24338-175-01) / 177.4 mL in 1 BOTTLE, PLASTICApr 1, 2026

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