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Olanzapine

NDC 71205-487, Olanzapine, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-487
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202862
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-487 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE15 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
71205-487-307120504873030 TABLET, FILM COATED in 1 BOTTLE (71205-487-30)
71205-487-607120504876060 TABLET, FILM COATED in 1 BOTTLE (71205-487-60)
71205-487-907120504879090 TABLET, FILM COATED in 1 BOTTLE (71205-487-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/61424fa3-b09a-4267-a208-a7c7c3f69fe5

Use it

Look up 71205-487 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-487 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-487. 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.