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Lubiprostone

NDC 76420-906, lubiprostone, capsule, gelatin coated, from Asclemed USA, Inc..

Product NDC
76420-906
Status
Listed
Labeler
Asclemed USA, Inc.
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/76420-906 \
  -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
76420-906-0176420090601100 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-01)
76420-906-307642009063030 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-30)
76420-906-607642009066060 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-60)
76420-906-907642009069090 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f5653f3b-c3c8-487c-bc00-3770985aa5ee

Use it

Look up 76420-906 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-906 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-906. 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.