Skip to content
healthcare.dev

SUPREP Bowel Prep

NDC 24338-175, sodium sulfate, potassium sulfate, magnesium sulfate, solution, concentrate, from Azurity Pharmaceuticals, Inc..

Product NDC
24338-175
Status
Listed
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
SOLUTION, CONCENTRATE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA022372
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24338-175 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM SULFATE17.5 g/mL
  • POTASSIUM SULFATE3.13 g/mL
  • MAGNESIUM SULFATE, UNSPECIFIED FORM1.6 g/mL

Pharmacologic classes

Calculi Dissolution Agent [EPC]; Increased Large Intestinal Motility [PE]; Increased Large Intestinal Motility [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Potassium Compounds [CS]; Potassium Salt [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Package NDCNDC-11Package
24338-175-01243380175012 BOTTLE, PLASTIC in 1 CARTON (24338-175-01) / 177.4 mL in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

Use it

Look up 24338-175 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24338-175 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24338-175. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.