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Prucalopride

NDC 60505-4806, Prucalopride, tablet, film coated, from Apotex Corp..

Product NDC
60505-4806
Status
Listed
Labeler
Apotex Corp.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218977
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60505-4806 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRUCALOPRIDE SUCCINATE1 mg/1

Pharmacologic classes

Serotonin 4 Receptor Agonists [MoA]; Serotonin-4 Receptor Agonist [EPC]

Package NDCNDC-11Package
60505-4806-36050548060330 TABLET, FILM COATED in 1 BOTTLE (60505-4806-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/01dcea95-b391-79da-bbfe-412f39022e9a
  • NADAC price for package 60505480603

    GET /v1/drugs/nadac/60505480603

Use it

Look up 60505-4806 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60505-4806 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60505-4806. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.