NDC 42571-268 – Tofacitinib

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

Human Prescription Drug

Product NDC42571-268

Product details

Brand name
Tofacitinib
Generic name
Tofacitinib
Labeler
Micro Labs Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209738
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 (4)

Package NDCDescriptionSince
42571-268-05500 TABLET, FILM COATED in 1 BOTTLE (42571-268-05)Jun 3, 2026
42571-268-3030 TABLET, FILM COATED in 1 BOTTLE (42571-268-30)Jun 3, 2026
42571-268-6060 TABLET, FILM COATED in 1 BOTTLE (42571-268-60)Jun 3, 2026
42571-268-76150 BLISTER PACK in 1 CARTON (42571-268-76) / 15 TABLET, FILM COATED in 1 BLISTER PACK (42571-268-13)Jun 3, 2026

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