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Chlorpromazine hydrochloride

NDC 70710-1129, Chlorpromazine hydrochloride, tablet, film coated, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
70710-1129
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213368
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1129 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLORPROMAZINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
70710-1129-170710112901100 TABLET, FILM COATED in 1 BOTTLE (70710-1129-1)
70710-1129-47071011290410 BLISTER PACK in 1 CARTON (70710-1129-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1129-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fc2bd95d-a7bc-4ab5-bffa-f5059cb8eb63

  • NADAC price for package 70710112901

    GET /v1/drugs/nadac/70710112901

Use it

Look up 70710-1129 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1129 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1129. 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.