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Prochlorperazine

NDC 54348-989, PROCHLORPERAZINE, tablet, from PharmPak, Inc..

Product NDC
54348-989
Status
Listed
Labeler
PharmPak, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040268
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/54348-989 \
  -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
54348-989-06543480989061 BOTTLE in 1 BOX (54348-989-06) / 6 TABLET in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/383744db-ba57-478a-8041-2ecc26d3e1ec

Use it

Look up 54348-989 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/54348-989 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 54348-989. 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.