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Chlorpromazine hydrochloride

NDC 73043-049, Chlorpromazine hydrochloride, injection, from Devatis, Inc..

Product NDC
73043-049
Status
Listed
Labeler
Devatis, Inc.
Dosage form
INJECTION
Route
INTRAMUSCULAR
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218229
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73043-049 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLORPROMAZINE HYDROCHLORIDE25 mg/mL

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
73043-049-257304300492525 AMPULE in 1 CARTON (73043-049-25) / 2 mL in 1 AMPULE (73043-049-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b73b9044-7132-41b7-83d4-2d135ea831f1

Use it

Look up 73043-049 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73043-049 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73043-049. 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.