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Lurasidone Hydrochloride

NDC 76282-534, Lurasidone Hydrochloride, tablet, film coated, from Exelan Pharmaceuticals Inc..

Product NDC
76282-534
Status
Listed
Labeler
Exelan Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208028
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76282-534 \
  -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
76282-534-307628205343030 TABLET, FILM COATED in 1 BOTTLE (76282-534-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4223e7f8-acbb-4738-9b77-ddc3405afb25

  • NADAC price for package 76282053430

    GET /v1/drugs/nadac/76282053430

Use it

Look up 76282-534 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76282-534 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76282-534. 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.