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PALIPERIDONE

NDC 43975-351, PALIPERIDONE, tablet, extended release, from ANI Pharmaceuticals, Inc..

Product NDC
43975-351
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204452
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43975-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PALIPERIDONE6 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
43975-351-034397503510330 TABLET, EXTENDED RELEASE in 1 BOTTLE (43975-351-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bbbaa057-f587-4eb9-a0d2-463dbcd57661

  • NADAC price for package 43975035103

    GET /v1/drugs/nadac/43975035103

Use it

Look up 43975-351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43975-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43975-351. 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.