United States · FDA National Drug Code directory

TOFACITINIB

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
59651-685_495ffb70-86d7-4a66-bf77-5ae7776ef9e6
Product NDC
59651-685
Form
TABLET, EXTENDED RELEASE
Composition / generic term
TOFACITINIB
Labeler
Aurobindo Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20260603
Source listing expiry
20271231

Source-listed ingredients

  • TOFACITINIB CITRATE — 11 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-685-30) · 59651-685-30

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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