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Lubiprostone

NDC 82804-304, Lubiprostone, capsule, gelatin coated, from Proficient Rx LP.

Product NDC
82804-304
Status
Listed
Labeler
Proficient Rx LP
Dosage form
CAPSULE, GELATIN COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209920
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82804-304 \
  -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
82804-304-608280403046060 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-304-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5fd683a5-87ff-42b8-a8c8-fff81625f67f

Use it

Look up 82804-304 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-304 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-304. 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.