NDC 70069-842 – Tofacitinib

Tofacitinib Citrate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70069-842

Product details

Brand name
Tofacitinib
Generic name
Tofacitinib
Labeler
Somerset Therapeutics, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA220137
Marketed since
June 3, 2026
Listing expires
December 31, 2027
Pharmacologic class
Janus Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tofacitinib →

Package NDC codes (1)

Package NDCDescriptionSince
70069-842-0160 TABLET, FILM COATED in 1 BOTTLE (70069-842-01)Jun 3, 2026

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