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OLANZAPINE

NDC 72303-0836, Olanzapine, tablet, from HEC Pharm USA Inc..

Product NDC
72303-0836
Status
Listed
Labeler
HEC Pharm USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206238
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72303-0836 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE5 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
72303-0836-17230308360130 TABLET in 1 BOTTLE, PLASTIC (72303-0836-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4d34f8f3-edc8-0a68-e063-6394a90a9c1f

  • NADAC price for package 72303083601

    GET /v1/drugs/nadac/72303083601

Use it

Look up 72303-0836 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72303-0836 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72303-0836. 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.