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NDC 24338-236, Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, powder, for solution, from Azurity Pharmaceuticals, Inc..

Product NDC
24338-236
Status
Listed
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA019011
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24338-236 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POLYETHYLENE GLYCOL 3350236 g/4L
  • SODIUM SULFATE ANHYDROUS22.74 g/4L
  • SODIUM BICARBONATE6.74 g/4L
  • SODIUM CHLORIDE5.86 g/4L
  • POTASSIUM CHLORIDE2.97 g/4L

Pharmacologic classes

Increased Large Intestinal Motility [PE]; 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 Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; 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
24338-236-01243380236014 L in 1 BOTTLE, PLASTIC (24338-236-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7609ecf7-0ce0-4fbb-9c27-30987f689575

  • NADAC price for package 24338023601

    GET /v1/drugs/nadac/24338023601

Use it

Look up 24338-236 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24338-236 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24338-236. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.