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PRUCALOPRIDE

NDC 0781-8159, PRUCALOPRIDE, tablet, film coated, from Sandoz Inc..

Product NDC
0781-8159
Status
Listed
Labeler
Sandoz Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218963
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-8159 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRUCALOPRIDE SUCCINATE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0781-8159-310078181593130 TABLET, FILM COATED in 1 BOTTLE (0781-8159-31)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6325308c-4b0f-4926-bb85-b63db614533d

  • NADAC price for package 00781815931

    GET /v1/drugs/nadac/00781815931

Use it

Look up 0781-8159 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-8159 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-8159. 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.