upadacitinib extended-release tablets,
for oral use Initial U.S. Approval: 2019
As specified in the prescribing information, upadacitinib tablets is indicated for the treatment of rheumatoid arthritis. RINVOQis a Janus kinase (JAK) inhibitor indicated for the treatment of adults with moderately to severely active rheumatoid arthritis who have had an inadequate response or intolerance to methotrexate. (1) Limitation of Use: Use of RINVOQ in combination with other JAK inhibitors, biologic DMARDs, or with potent immunosuppressants such as azathioprine and cyclosporine is not recommended.
Facts about upadacitinib tablets
Approval Date: 2019
Proprietary Name: RINVOQ (upadacitinib) extended-release tablets
Active Ingredient(s): upadacitinib
FDA-approved use: rheumatoid arthritis
Dosage Form: Extended-release tablets: 15 mg
Medicine Approved By: US FDA
Manufacturer: AbbVie Inc.
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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Query For upadacitinib tablets
Approved accessible "upadacitinib tablets"
Rinvoq (upadacitinib) tablets were originally approved in 2019. In 2022, Rinvoq was approved to treat adults with moderately to severely active ulcerative colitis who have had an inadequate response or intolerance to another type of treatment. Ulcerative colitis is a type of inflammatory bowel disease.
RINVOQis a prescription medicine that is a Janus kinase (JAK) inhibitor. RINVOQ is used to treat adults with moderate to severe rheumatoid arthritis in whom methotrexate did not work well or could not be tolerated. It is not known if RINVOQ is safe and effective in children under 18 years of age. Active ingredient: upadacitinib Inactive ingredients: microcrystalline cellulose, hypromellose, mannitol, tartaric acid, colloidal silicon dioxide, magnesium stearate, polyvinyl alcohol, polyethylene glycol, talc, titanium dioxide, ferrosoferric oxide, and iron oxide red.
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RINVOQ (upadacitinib) extended-release tablets, for oral use Initial U.S. Approval: 2019
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