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Lurasidone Hydrochloride

NDC 43598-355, Lurasidone Hydrochloride, tablet, film coated, from Dr. Reddys Laboratories Inc.

Product NDC
43598-355
Status
Listed
Labeler
Dr. Reddys Laboratories Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208055
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-355 \
  -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
43598-355-304359803553030 TABLET, FILM COATED in 1 BOTTLE (43598-355-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2f22a0bd-94f3-53d7-717c-03da8e1a7e97

  • NADAC price for package 43598035530

    GET /v1/drugs/nadac/43598035530

Use it

Look up 43598-355 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-355 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-355. 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.