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Lurasidone Hydrochloride

NDC 47335-639, Lurasidone Hydrochloride, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-639
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208066
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-639 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LURASIDONE HYDROCHLORIDE60 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
47335-639-1347335063913500 TABLET in 1 BOTTLE (47335-639-13)
47335-639-814733506398190 TABLET in 1 BOTTLE (47335-639-81)
47335-639-834733506398330 TABLET in 1 BOTTLE (47335-639-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6d97d871-66d3-4ed8-bbc5-0620e9f69ae5

  • NADAC price for package 47335063983

    GET /v1/drugs/nadac/47335063983

Use it

Look up 47335-639 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-639 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-639. 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.