NDC 70710-1727 – Tofacitinib

Tofacitinib Citrate 22 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

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

Uses, dosage, side effects and warnings for Tofacitinib →

Package NDC codes (2)

Package NDCDescriptionSince
70710-1727-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1727-3)May 20, 2026
70710-1727-990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1727-9)May 20, 2026

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