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Olanzapine

NDC 65862-659, Olanzapine, tablet, orally disintegrating, from Aurobindo Pharma Limited.

Product NDC
65862-659
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203708
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-659 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE20 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
65862-659-03658620659033 BLISTER PACK in 1 CARTON (65862-659-03) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-659-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4d768cfe-3b20-4127-95b9-b4151b28afcc

Use it

Look up 65862-659 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-659 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-659. 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.