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Lubiprostone

NDC 63304-351, lubiprostone, capsule, gelatin coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
63304-351
Status
Listed
Labeler
Sun Pharmaceutical Industries, 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/63304-351 \
  -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
63304-351-606330403516060 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-351-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f06d76d2-028a-629f-e053-2995a90a80f5

  • NADAC price for package 63304035160

    GET /v1/drugs/nadac/63304035160

Use it

Look up 63304-351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-351. 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.