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Lurasidone hydrochloride

NDC 68382-859, Lurasidone hydrochloride, tablet, coated, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-859
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208052
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-859 \
  -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
68382-859-0168382085901100 TABLET, COATED in 1 BOTTLE (68382-859-01)
68382-859-0568382085905500 TABLET, COATED in 1 BOTTLE (68382-859-05)
68382-859-066838208590630 TABLET, COATED in 1 BOTTLE (68382-859-06)
68382-859-166838208591690 TABLET, COATED in 1 BOTTLE (68382-859-16)
68382-859-7768382085977100 BLISTER PACK in 1 CARTON (68382-859-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-859-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bceb350e-4b88-4de1-9629-9629365a27a7
  • NADAC price for package 68382085906

    GET /v1/drugs/nadac/68382085906

Use it

Look up 68382-859 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-859 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-859. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.