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Olanzapine

NDC 60505-3112, Olanzapine, tablet, film coated, from Apotex Corp..

Product NDC
60505-3112
Status
Listed
Labeler
Apotex Corp.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090798
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60505-3112 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE7.5 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
60505-3112-06050531120010 BLISTER PACK in 1 CARTON (60505-3112-0) / 10 TABLET, FILM COATED in 1 BLISTER PACK
60505-3112-8605053112081000 TABLET, FILM COATED in 1 BOTTLE (60505-3112-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3347d1c8-04c9-5ce1-8cda-b38e0412b709

  • NADAC price for package 60505311200

    GET /v1/drugs/nadac/60505311200

  • NADAC price for package 60505311208

    GET /v1/drugs/nadac/60505311208

Use it

Look up 60505-3112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60505-3112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60505-3112. 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.