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Olanzapine

NDC 65862-566, Olanzapine, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-566
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202050
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-566 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE20 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
65862-566-0165862056601100 TABLET in 1 BOTTLE (65862-566-01)
65862-566-0565862056605500 TABLET in 1 BOTTLE (65862-566-05)
65862-566-106586205661010 BLISTER PACK in 1 CARTON (65862-566-10) / 10 TABLET in 1 BLISTER PACK
65862-566-306586205663030 TABLET in 1 BOTTLE (65862-566-30)
65862-566-99658620566991000 TABLET in 1 BOTTLE (65862-566-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/636665be-9d7e-443a-8134-e8cc47e6ba24

Use it

Look up 65862-566 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-566 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-566. 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.