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lurasidone hydrochloride

NDC 72205-210, lurasidone hydrochloride, tablet, film coated, from Novadoz Pharmaceuticals LLC.

Product NDC
72205-210
Status
Listed
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208037
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72205-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LURASIDONE HYDROCHLORIDE80 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
72205-210-0572205021005500 TABLET, FILM COATED in 1 BOTTLE (72205-210-05)
72205-210-307220502103030 TABLET, FILM COATED in 1 BOTTLE (72205-210-30)
72205-210-907220502109090 TABLET, FILM COATED in 1 BOTTLE (72205-210-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4f969224-a9f0-4089-84d6-a15664ea7bfe

  • NADAC price for package 72205021030

    GET /v1/drugs/nadac/72205021030

Use it

Look up 72205-210 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72205-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72205-210. 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.