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lurasidone hydrochloride

NDC 16729-349, lurasidone hydrochloride, tablet, film coated, from Accord Healthcare, Inc..

Product NDC
16729-349
Status
Listed
Labeler
Accord Healthcare, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208049
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16729-349 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LURASIDONE HYDROCHLORIDE80 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
16729-349-101672903491030 TABLET, FILM COATED in 1 BOTTLE (16729-349-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7e11ec22-63c1-41a6-899c-4fe746f76bd0

Use it

Look up 16729-349 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16729-349 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16729-349. 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.