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Lurasidone Hydrochloride

NDC 69097-942, Lurasidone Hydrochloride, tablet, film coated, from Cipla USA, Inc..

Product NDC
69097-942
Status
Listed
Labeler
Cipla USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208028
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-942 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LURASIDONE HYDROCHLORIDE20 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
69097-942-026909709420230 TABLET, FILM COATED in 1 BOTTLE (69097-942-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/76c055aa-d96a-42e5-a670-1db63b9c1dd6

Use it

Look up 69097-942 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-942 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-942. 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.