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Lubiprostone

NDC 82804-001, Lubiprostone, capsule, gelatin coated, from Proficient Rx LP.

Product NDC
82804-001
Status
Listed
Labeler
Proficient Rx LP
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/82804-001 \
  -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
82804-001-308280400013030 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-001-30)
82804-001-608280400016060 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-001-60)
82804-001-908280400019090 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-001-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/34c547c4-4c29-45a9-97c7-a828bf2ecde0

Use it

Look up 82804-001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-001. 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.