NDC 70710-1727 – Tofacitinib
Tofacitinib Citrate 22 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70710-1727
Product details
- Brand name
- Tofacitinib
- Generic name
- Tofacitinib
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA214264
- Marketed since
- May 20, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Janus Kinase Inhibitor
Active ingredients
- Tofacitinib Citrate 22 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1727-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1727-3) | May 20, 2026 |
| 70710-1727-9 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1727-9) | May 20, 2026 |
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