NDC 70069-841

Tofacitinib 5 mg tablet, film coated

On the label: Somerset Therapeutics, LLC.

Portugal: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Bluepharma - IndÚstria FarmacÊutica, S.a.Coimbra, PortugalMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 9, 2025 · 7 inspections

Product details

Generic drug
Tofacitinib: every company that makes it
Form
tablet, film coated, oral
Strength
5 mg
Approval
ANDA ANDA220137
On the market since
Jun 3, 2026
Package NDCs
70069-841-01
Official label
DailyMed (National Library of Medicine), updated Jun 2, 2026

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