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PROCHLORPERAZINE MALEATE

NDC 69315-265, PROCHLORPERAZINE MALEATE, tablet, film coated, from Leading Pharma, LLC.

Product NDC
69315-265
Status
Listed
Labeler
Leading Pharma, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218912
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69315-265 \
  -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
69315-265-0169315026501100 TABLET, FILM COATED in 1 BOTTLE (69315-265-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c93494ef-c510-4e46-a1b1-362624200223

  • NADAC price for package 69315026501

    GET /v1/drugs/nadac/69315026501

Use it

Look up 69315-265 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69315-265 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69315-265. 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.