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TOFACITINIB

NDC 70069-842, TOFACITINIB, tablet, film coated, from Somerset Therapeutics, LLC.

Product NDC
70069-842
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA220137
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-842 \
  -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
70069-842-017006908420160 TABLET, FILM COATED in 1 BOTTLE (70069-842-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2726c2b0-c763-4635-ac6b-4334c3a5a8bc

Use it

Look up 70069-842 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-842 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-842. 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.