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Olanzapine

NDC 65862-565, Olanzapine, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-565
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/65862-565 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE15 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
65862-565-0165862056501100 TABLET in 1 BOTTLE (65862-565-01)
65862-565-106586205651010 BLISTER PACK in 1 CARTON (65862-565-10) / 10 TABLET in 1 BLISTER PACK
65862-565-306586205653030 TABLET in 1 BOTTLE (65862-565-30)
65862-565-99658620565991000 TABLET in 1 BOTTLE (65862-565-99)

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 65862-565 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-565 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-565. 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.