NDC 70710-1589 – Tofacitinib
Tofacitinib Citrate 10 mg/1 · Tablet, Film Coated · Oral
Product NDC70710-1589
Product details
- Brand name
- Tofacitinib
- Generic name
- Tofacitinib
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209829
- Marketed since
- June 5, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Janus Kinase Inhibitor
Active ingredients
- Tofacitinib Citrate 10 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1589-6 | 60 TABLET, FILM COATED in 1 BOTTLE (70710-1589-6) | Jun 5, 2026 |
| 70710-1589-7 | 28 TABLET, FILM COATED in 1 BOTTLE (70710-1589-7) | Jun 5, 2026 |
| 70710-1589-8 | 180 TABLET, FILM COATED in 1 BOTTLE (70710-1589-8) | Jun 5, 2026 |
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