United States · FDA National Drug Code directory

XELJANZ

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
0069-1001_40c4e5e1-3891-4949-bd0e-db319cc1e813
Product NDC
0069-1001
Form
TABLET, FILM COATED
Composition / generic term
tofacitinib
Labeler
Pfizer Laboratories Div Pfizer Inc
Marketing category
NDA
Marketing start / end (source format)
20121109
Source listing expiry
20271231

Source-listed ingredients

  • TOFACITINIB CITRATE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, FILM COATED in 1 BOTTLE (0069-1001-01) · 0069-1001-01

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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