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Ziprasidone Hydrochloride

NDC 65862-705, Ziprasidone Hydrochloride, capsule, from Aurobindo Pharma Limited.

Product NDC
65862-705
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204117
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-705 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZIPRASIDONE HYDROCHLORIDE80 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
65862-705-606586207056060 CAPSULE in 1 BOTTLE (65862-705-60)
65862-705-80658620705808 BLISTER PACK in 1 CARTON (65862-705-80) / 10 CAPSULE in 1 BLISTER PACK (65862-705-10)
65862-705-99658620705991000 CAPSULE in 1 BOTTLE (65862-705-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cc5e1c44-79e9-45d3-b1e5-b003f550c508

  • NADAC price for package 65862070560

    GET /v1/drugs/nadac/65862070560

Use it

Look up 65862-705 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-705 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-705. 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.