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Lurasidone Hydrochloride

NDC 53746-880, Lurasidone Hydrochloride, tablet, coated, from Amneal Pharmaceuticals of New York LLC.

Product NDC
53746-880
Status
Listed
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208002
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/53746-880 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LURASIDONE HYDROCHLORIDE40 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
53746-880-305374608803030 TABLET, COATED in 1 BOTTLE (53746-880-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/84648adf-b3c6-476e-8d11-2a9d7c5eb550

Use it

Look up 53746-880 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/53746-880 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 53746-880. 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.