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Tofacitinib

NDC 72205-140, Tofacitinib, tablet, film coated, from Novadoz Pharmaceuticals LLC.

Product NDC
72205-140
Status
Listed
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217299
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72205-140 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TOFACITINIB CITRATE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72205-140-1872205014018180 TABLET, FILM COATED in 1 BOTTLE (72205-140-18)
72205-140-287220501402828 TABLET, FILM COATED in 1 BOTTLE (72205-140-28)
72205-140-607220501406060 TABLET, FILM COATED in 1 BOTTLE (72205-140-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/253635c8-1ea7-41ba-b216-dea5e3305c47

Use it

Look up 72205-140 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72205-140 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72205-140. 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.