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Chlorpromazine Hydrochloride

NDC 70518-4142, Chlorpromazine Hydrochloride, tablet, sugar coated, from REMEDYREPACK INC..

Product NDC
70518-4142
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, SUGAR COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214827
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4142 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLORPROMAZINE HYDROCHLORIDE200 mg/1

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
70518-4142-070518414200100 POUCH in 1 BOX (70518-4142-0) / 1 TABLET, SUGAR COATED in 1 POUCH (70518-4142-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b8137906-946c-455d-87c0-0e130cd9266f

Use it

Look up 70518-4142 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4142 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4142. 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.