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Prochlorperazine Maleate

NDC 70710-1667, Prochlorperazine Maleate, tablet, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
70710-1667
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216495
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1667 \
  -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
70710-1667-170710166701100 TABLET in 1 BOTTLE (70710-1667-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d4a34138-a01b-418f-8e0f-e81f6e1cfd89

  • NADAC price for package 70710166701

    GET /v1/drugs/nadac/70710166701

Use it

Look up 70710-1667 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1667 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1667. 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.