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Olanzapine

NDC 72789-460, Olanzapine, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-460
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076255
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-460 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE5 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
72789-460-147278904601414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-460-14)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/10043041-a632-4e57-bc08-37216dea8546

Use it

Look up 72789-460 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-460 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-460. 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.