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Chlorpromazine Hydrochloride

NDC 59651-570, Chlorpromazine Hydrochloride, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-570
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216788
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-570 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLORPROMAZINE HYDROCHLORIDE100 mg/1

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
59651-570-0159651057001100 TABLET in 1 BOTTLE (59651-570-01)
59651-570-99596510570991000 TABLET in 1 BOTTLE (59651-570-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c2a8b8a3-187f-4000-bde3-b40bb0e5600f

Use it

Look up 59651-570 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-570 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-570. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.