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Lactulose

NDC 18124-002, Lactulose, solution, from Fresenius Kabi Austria GmbH.

Product NDC
18124-002
Status
Listed
Labeler
Fresenius Kabi Austria GmbH
Dosage form
SOLUTION
Route
ORAL, RECTAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090502
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/18124-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LACTULOSE10 g/15mL

Pharmacologic classes

Acidifying Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Package NDCNDC-11Package
18124-002-1618124000216473 mL in 1 BOTTLE (18124-002-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a89835c9-8ce5-4627-8d7d-70ff175b2e07

Use it

Look up 18124-002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/18124-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 18124-002. 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.