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Lurasidone hydrochloride

NDC 70771-1734, Lurasidone hydrochloride, tablet, coated, from Zydus Lifesciences Limited.

Product NDC
70771-1734
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208052
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1734 \
  -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
70771-1734-170771173401100 TABLET, COATED in 1 BOTTLE (70771-1734-1)
70771-1734-37077117340330 TABLET, COATED in 1 BOTTLE (70771-1734-3)
70771-1734-47077117340410 BLISTER PACK in 1 CARTON (70771-1734-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1734-2)
70771-1734-570771173405500 TABLET, COATED in 1 BOTTLE (70771-1734-5)
70771-1734-97077117340990 TABLET, COATED in 1 BOTTLE (70771-1734-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0f5f8228-1304-4981-8577-029136627260

Use it

Look up 70771-1734 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1734 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1734. 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.