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Lurasidone Hydrochloride

NDC 31722-084, Lurasidone Hydrochloride, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-084
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218174
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-084 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LURASIDONE HYDROCHLORIDE120 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
31722-084-0531722008405500 TABLET, FILM COATED in 1 BOTTLE (31722-084-05)
31722-084-303172200843030 TABLET, FILM COATED in 1 BOTTLE (31722-084-30)
31722-084-903172200849090 TABLET, FILM COATED in 1 BOTTLE (31722-084-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c80625bb-7857-4763-81fe-542b3448d84f

  • NADAC price for package 31722008430

    GET /v1/drugs/nadac/31722008430

Use it

Look up 31722-084 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-084 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-084. 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.