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tofacitinib

NDC 70771-1967, tofacitinib, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1967
Status
Listed
Labeler
Zydus Lifesciences Limited
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/70771-1967 \
  -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
70771-1967-67077119670660 TABLET, FILM COATED in 1 BOTTLE (70771-1967-6)
70771-1967-77077119670728 TABLET, FILM COATED in 1 BOTTLE (70771-1967-7)
70771-1967-870771196708180 TABLET, FILM COATED in 1 BOTTLE (70771-1967-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f4d0e580-74a8-496e-89a2-d74478c946bf

Use it

Look up 70771-1967 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1967 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1967. 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.