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Lurasidone Hydrochloride

NDC 23155-888, Lurasidone Hydrochloride, tablet, film coated, from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..

Product NDC
23155-888
Status
Listed
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208058
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/23155-888 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LURASIDONE HYDROCHLORIDE40 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
23155-888-032315508880330 TABLET, FILM COATED in 1 BOTTLE (23155-888-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/083a1a52-5a13-4e28-8ef2-127ac4ce5b2d

  • NADAC price for package 23155088803

    GET /v1/drugs/nadac/23155088803

Use it

Look up 23155-888 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/23155-888 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 23155-888. 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.