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Olanzapine

NDC 82804-067, Olanzapine, tablet, film coated, from Proficient Rx LP.

Product NDC
82804-067
Status
Listed
Labeler
Proficient Rx LP
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/82804-067 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE20 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
82804-067-308280400673030 TABLET, FILM COATED in 1 BOTTLE (82804-067-30)
82804-067-608280400676060 TABLET, FILM COATED in 1 BOTTLE (82804-067-60)
82804-067-908280400679090 TABLET, FILM COATED in 1 BOTTLE (82804-067-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/024e8e9b-a4fc-4882-b080-c070467166a6

Use it

Look up 82804-067 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-067 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-067. 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.