United States · FDA National Drug Code directory

XELJANZ XR

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
63539-502_e8ed9fec-0cc3-403c-a731-72a6f8969afa
Product NDC
63539-502
Form
TABLET, EXTENDED RELEASE
Composition / generic term
tofacitinib
Labeler
U.S. Pharmaceuticals
Marketing category
NDA
Marketing start / end (source format)
20200121
Source listing expiry
20271231

Source-listed ingredients

  • TOFACITINIB CITRATE — 22 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63539-502-30) · 63539-502-30

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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