Product/Composition:- | Upadacitinib tablets |
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Strength:- | 15 mg, 30 mg |
Form:- | Tablets |
Reference Brands:- | Rinvoq(US & EU) |
MOQ | As per the manufacturer batch size |
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Upadacitinib inhibits Janus kinase (JAK) enzymes, blocking cytokine signaling involved in inflammation. It effectively reduces symptoms and disease progression in rheumatoid arthritis. Benefits include rapid relief, improved joint function, and better quality of life, with convenient oral dosing and a safety profile suitable for long-term autoimmune therapy when monitored properly.
Upadacitinib tablets are approved in the EU and US for moderate to severe rheumatoid arthritis. In the EU, AbbVie’s Rinvoq is regulated by EMA, supported by dossiers demonstrating safety, efficacy, and quality manufacturing. In the US, FDA approval is based on extensive clinical trial data, biosimilarity, and pharmacovigilance. Both regions require detailed dossiers for initial approval and ongoing safety monitoring. For expert assistance with regulatory dossiers, compliance, and registration, visit PharmaTradz. We support efficient market access for upadacitinib tablets, ensuring adherence to European and American standards for safe, effective autoimmune disease management, helping you navigate complex regulatory processes seamlessly.