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tofacitinib

NDC 70710-1589, tofacitinib, tablet, film coated, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1589
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209829
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1589 \
  -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
70710-1589-67071015890660 TABLET, FILM COATED in 1 BOTTLE (70710-1589-6)
70710-1589-77071015890728 TABLET, FILM COATED in 1 BOTTLE (70710-1589-7)
70710-1589-870710158908180 TABLET, FILM COATED in 1 BOTTLE (70710-1589-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/21a89264-8047-40ac-8b10-fa6461072509

Use it

Look up 70710-1589 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1589 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1589. 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.