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Chlorpromazine Hydrochloride

NDC 70710-1850, Chlorpromazine Hydrochloride, injection, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1850
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
INTRAMUSCULAR
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217275
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1850 \
  -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
70710-1850-77071018500725 VIAL in 1 CARTON (70710-1850-7) / 2 mL in 1 VIAL (70710-1850-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7cd6dc0d-e98d-40ae-80d4-c15f63056abf

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70710-1850

Use it

Look up 70710-1850 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1850 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1850. 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.