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Olanzapine

NDC 68788-8722, Olanzapine, tablet, film coated, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8722
Status
Listed
Labeler
Preferred 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/68788-8722 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE5 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
68788-8722-36878887220330 TABLET, FILM COATED in 1 BOTTLE (68788-8722-3)
68788-8722-66878887220660 TABLET, FILM COATED in 1 BOTTLE (68788-8722-6)
68788-8722-96878887220990 TABLET, FILM COATED in 1 BOTTLE (68788-8722-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d349d5b7-5658-46d6-9bba-e6f6361cebb9

Use it

Look up 68788-8722 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8722 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8722. 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.