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PROCHLORPERAZINE MALEATE

NDC 69452-471, Prochlorperazine Maleate, tablet, from Bionpharma Inc..

Product NDC
69452-471
Status
Listed
Labeler
Bionpharma Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217478
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69452-471 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROCHLORPERAZINE MALEATE5 mg/1

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
69452-471-2069452047120100 TABLET in 1 BOTTLE (69452-471-20)
69452-471-32694520471321000 TABLET in 1 BOTTLE (69452-471-32)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2cf363d6-b9e4-2c22-e063-6394a90a7649

  • NADAC price for package 69452047120

    GET /v1/drugs/nadac/69452047120

Use it

Look up 69452-471 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69452-471 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69452-471. 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.