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NDC 24338-550, polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution, kit, from Azurity Pharmaceuticals, Inc..

Product NDC
24338-550
Status
Listed
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
KIT
Route
—
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA215344
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24338-550 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
24338-550-01243380550011 KIT in 1 KIT (24338-550-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d5710a04-2b0a-402c-a8b0-025766f1a437

  • NADAC price for package 24338055001

    GET /v1/drugs/nadac/24338055001

Use it

Look up 24338-550 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24338-550 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24338-550. 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.