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Chlorpromazine Hydrochloride

NDC 71656-102, Chlorpromazine Hydrochloride, concentrate, from Saptalis Pharmaceuticals, LLC..

Product NDC
71656-102
Status
Listed
Labeler
Saptalis Pharmaceuticals, LLC.
Dosage form
CONCENTRATE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA080983
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71656-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLORPROMAZINE HYDROCHLORIDE30 mg/mL

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
71656-102-0471656010204120 mL in 1 BOTTLE, PLASTIC (71656-102-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cd8f9e23-d08a-4d96-8fe9-35ab2bc861c8

Use it

Look up 71656-102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71656-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71656-102. 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.