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Lurasidone Hydrochloride

NDC 13668-737, Lurasidone Hydrochloride, tablet, film coated, from Torrent Pharmaceuticals Limited.

Product NDC
13668-737
Status
Listed
Labeler
Torrent Pharmaceuticals Limited
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/13668-737 \
  -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
13668-737-301366807373030 TABLET, FILM COATED in 1 BOTTLE (13668-737-30)
13668-737-901366807379090 TABLET, FILM COATED in 1 BOTTLE (13668-737-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9cb5e275-1029-407a-8c93-ec5cde2d323b

Use it

Look up 13668-737 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/13668-737 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 13668-737. 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.