NDC 70710-1243 – Tofacitinib

Tofacitinib Citrate 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70710-1243

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
May 11, 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
70710-1243-660 TABLET, FILM COATED in 1 BOTTLE (70710-1243-6)May 11, 2026
70710-1243-8180 TABLET, FILM COATED in 1 BOTTLE (70710-1243-8)May 11, 2026

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