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Haloperidol

NDC 68382-408, Haloperidol, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-408
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
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/68382-408 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HALOPERIDOL1 mg/1

Pharmacologic classes

Typical Antipsychotic [EPC]

Package NDCNDC-11Package
68382-408-0168382040801100 TABLET in 1 BOTTLE (68382-408-01)
68382-408-10683820408101000 TABLET in 1 BOTTLE (68382-408-10)
68382-408-776838204087710 BLISTER PACK in 1 CARTON (68382-408-77) / 10 TABLET in 1 BLISTER PACK (68382-408-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/54502f78-7244-454a-9171-4e73127f1456

  • NADAC price for package 68382040801

    GET /v1/drugs/nadac/68382040801

Use it

Look up 68382-408 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-408 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-408. 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.