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Haloperidol

NDC 65841-837, Haloperidol, tablet, from Zydus Lifesciences Limited.

Product NDC
65841-837
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077580
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65841-837 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HALOPERIDOL.5 mg/1

Pharmacologic classes

Typical Antipsychotic [EPC]

Package NDCNDC-11Package
65841-837-0165841083701100 TABLET in 1 BOTTLE (65841-837-01)
65841-837-10658410837101000 TABLET in 1 BOTTLE (65841-837-10)
65841-837-776584108377710 BLISTER PACK in 1 CARTON (65841-837-77) / 10 TABLET in 1 BLISTER PACK (65841-837-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/509d0eb2-b930-4836-9669-dbebf0ac4076

Use it

Look up 65841-837 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-837 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-837. 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.