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lurasidone hydrochloride

NDC 33342-422, lurasidone hydrochloride, tablet, film coated, from Macleods Pharmaceuticals Limited.

Product NDC
33342-422
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212124
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-422 \
  -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
33342-422-073334204220730 TABLET, FILM COATED in 1 BOTTLE (33342-422-07)
33342-422-103334204221090 TABLET, FILM COATED in 1 BOTTLE (33342-422-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2b07a830-93ba-427a-95fc-5138a6309f1e

  • NADAC price for package 33342042207

    GET /v1/drugs/nadac/33342042207

Use it

Look up 33342-422 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-422 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-422. 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.