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Paliperidone

NDC 47335-766, Paliperidone, tablet, film coated, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-766
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205618
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-766 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PALIPERIDONE6 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
47335-766-834733507668330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-766-83)
47335-766-8847335076688100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-766-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0dc3a9b2-2edf-4fa2-a949-459b4218e763

  • NADAC price for package 47335076683

    GET /v1/drugs/nadac/47335076683

Use it

Look up 47335-766 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-766 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-766. 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.