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NDC 63402-302, lurasidone hydrochloride, tablet, film coated, from Sumitomo Pharma America, Inc..

Product NDC
63402-302
Status
Listed
Labeler
Sumitomo Pharma America, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA200603
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63402-302 \
  -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
63402-302-04634020302044 BLISTER PACK in 1 CARTON (63402-302-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-07)
63402-302-106340203021010 BLISTER PACK in 1 CARTON (63402-302-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-01)
63402-302-306340203023030 TABLET, FILM COATED in 1 BOTTLE (63402-302-30)
63402-302-5063402030250500 TABLET, FILM COATED in 1 BOTTLE (63402-302-50)
63402-302-906340203029090 TABLET, FILM COATED in 1 BOTTLE (63402-302-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/afad3051-9df2-4c54-9684-e8262a133af8

  • NADAC price for package 63402030230

    GET /v1/drugs/nadac/63402030230

Use it

Look up 63402-302 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63402-302 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63402-302. 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.