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Chlorpromazine hydrochloride

NDC 70771-1509, Chlorpromazine hydrochloride, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1509
Status
Listed
Labeler
Zydus Lifesciences Limited
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/70771-1509 \
  -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
70771-1509-170771150901100 TABLET, FILM COATED in 1 BOTTLE (70771-1509-1)
70771-1509-47077115090410 BLISTER PACK in 1 CARTON (70771-1509-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1509-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0ea5e0c6-0062-4be3-96f2-62397da3e77d

Use it

Look up 70771-1509 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1509 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1509. 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.