United States · FDA National Drug Code directory

tofacitinib solution

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
0054-0821_b5f66dbf-b020-442e-bf19-4af33ac3c802
Product NDC
0054-0821
Form
SOLUTION
Composition / generic term
tofacitinib
Labeler
Hikma Pharmaceuticals USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20260603
Source listing expiry
20271231

Source-listed ingredients

  • TOFACITINIB CITRATE — 1 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (0054-0821-58) / 240 mL in 1 BOTTLE · 0054-0821-58

Source and coverage

Open FDA National Drug Code directory

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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