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Risperidone

NDC 69367-372, Risperidone, tablet, film coated, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-372
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078707
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-372 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RISPERIDONE3 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
69367-372-0569367037205500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-372-05)
69367-372-606936703726060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-372-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/07d43bf6-a695-453a-a5c7-9581effe585c

  • NADAC price for package 69367037205

    GET /v1/drugs/nadac/69367037205

  • NADAC price for package 69367037260

    GET /v1/drugs/nadac/69367037260

Use it

Look up 69367-372 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-372 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-372. 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.