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
- 70710-1589_1587462d-cea8-47f1-b679-504d4b460c3d
- Product NDC
- 70710-1589
- Form
- TABLET, FILM COATED
- Composition / generic term
- tofacitinib
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260605
- Source listing expiry
- 20271231
Source-listed ingredients
- TOFACITINIB CITRATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED in 1 BOTTLE (70710-1589-6) · 70710-1589-6
- 28 TABLET, FILM COATED in 1 BOTTLE (70710-1589-7) · 70710-1589-7
- 180 TABLET, FILM COATED in 1 BOTTLE (70710-1589-8) · 70710-1589-8
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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