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LUBIPROSTONE

NDC 69339-163, LUBIPROSTONE, capsule, gelatin coated, from Natco Pharma USA LLC.

Product NDC
69339-163
Status
Listed
Labeler
Natco Pharma USA 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/69339-163 \
  -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
69339-163-176933901631740 BLISTER PACK in 1 CARTON (69339-163-17) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (69339-163-98)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/10c7b62d-6c39-453c-8d9a-2f441725bc3b

  • NADAC price for package 69339016317

    GET /v1/drugs/nadac/69339016317

Use it

Look up 69339-163 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69339-163 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69339-163. 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.