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Lubiprostone

NDC 80425-0354, lubiprostone, capsule, gelatin coated, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0354
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
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/80425-0354 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LUBIPROSTONE8 ug/1

Pharmacologic classes

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

Package NDCNDC-11Package
80425-0354-28042503540260 CAPSULE, GELATIN COATED in 1 BOTTLE (80425-0354-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/031170a4-5f7d-b371-e063-6394a90ae21d

Use it

Look up 80425-0354 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0354 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0354. 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.