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Lubiprostone

NDC 72189-607, Lubiprostone, capsule, gelatin coated, from Direct Rx.

Product NDC
72189-607
Status
Listed
Labeler
Direct Rx
Dosage form
CAPSULE, GELATIN COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021908
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-607 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LUBIPROSTONE24 ug/1

Pharmacologic classes

Chloride Channel Activator [EPC]; Chloride Channel Activators [MoA]

Package NDCNDC-11Package
72189-607-607218906076060 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-607-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2bd6f613-64d0-0291-e063-6294a90a0238

Use it

Look up 72189-607 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-607 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-607. 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.