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Baricitinib

NDC 0002-6885, baricitinib, tablet, film coated, from Eli Lilly and Company.

Product NDC
0002-6885
Status
Listed
Labeler
Eli Lilly and Company
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
EMERGENCY USE AUTHORIZATION
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0002-6885 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BARICITINIB4 mg/1

Pharmacologic classes

Janus Kinase Inhibitor [EPC]; Janus Kinase Inhibitors [MoA]

Package NDCNDC-11Package
0002-6885-300000268853030 TABLET, FILM COATED in 1 BOTTLE (0002-6885-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7052c055-fedf-453b-86bc-01f5465eb157

Use it

Look up 0002-6885 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0002-6885 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0002-6885. 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.