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Lurasidone Hydrochloride

NDC 65162-882, Lurasidone Hydrochloride, tablet, coated, from Amneal Pharmaceuticals LLC.

Product NDC
65162-882
Status
Listed
Labeler
Amneal Pharmaceuticals 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/65162-882 \
  -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
65162-882-036516208820330 TABLET, COATED in 1 BOTTLE (65162-882-03)
65162-882-096516208820990 TABLET, COATED in 1 BOTTLE (65162-882-09)
65162-882-5065162088250500 TABLET, COATED in 1 BOTTLE (65162-882-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6ef0b2f9-9356-4f61-a2fa-e7c2c77a5d3a

Use it

Look up 65162-882 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-882 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-882. 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.