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The NEUPRO Transdermal Patch (Rotigotine) is a medicated patch used to treat Parkinson's disease and moderate-to-severe primary Restless Legs Syndrome. Parkinson's disease (PD) is a neurodegenerative disorder that can cause tremors, slow movement, stiffness, and balance problems. Restless Legs Syndrome is a disorder that causes you to want to move your legs. As a result of long-term RLS, you may feel unpleasant sensations such as aching, burning, itching, throbbing, or tugging. NEUPRO Transdermal Patch (Rotigotine) is classified as adopamine agonist. Fact Table Formula C19H25NOS License US DailyMed, EU EMA Bioavailability 37% Legal status Rx-Only Chemical Name Rotigotine Elimination half-life 5–7 hours Dosage (Strength) 1mg - 8mg (24 hours patches) Pregnancy Consult Doctor Brands Neupro Protein binding 92% PubChem CID 57537 MedlinePlus a607059 ChEBI 135351 ATC code N04BC09 DrugBank DB05271 KEGG D05768 Routes of administration Transdermal patch

Neupro Transdermal Patch (Rotigotine)

  • For Parkinson's disease, NEUPRO Transdermal Patch (Rotigotine) dosages range from 2 mg/24 hours to 8 mg/24 hours. For Restless Legs Syndrome, NEUPRO Transdermal Patch (Rotigotine) dosages range from 1 mg/24 hours to 3 mg/24 hours. NEUPRO should be applied to clean, dry, and undamaged skin once a day. It should be held firmly in place for 30 seconds. The patch should not be placed where it could be rubbed by clothing. Do not place the patch on the same site of skin more than once every 14 days.
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