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Tofacitinib

NDC 42799-970, Tofacitinib, tablet, film coated, extended release, from Edenbridge Pharmaceuticals LLC..

Product NDC
42799-970
Status
Listed
Labeler
Edenbridge Pharmaceuticals LLC.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218668
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42799-970 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TOFACITINIB CITRATE11 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
42799-970-304279909703030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42799-970-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/576722e5-6639-452d-a5c3-33a064f19481

  • NADAC price for package 42799097030

    GET /v1/drugs/nadac/42799097030

Use it

Look up 42799-970 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42799-970 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42799-970. 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.