Rotigotine Transdermal Patch
Rotigotine transdermal patch is a dopamine agonist skin patch used to treat Parkinson's disease and moderate-to-severe primary Restless Legs Syndrome.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 1 clinical label set within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Neupro (rotigotine) is a once-daily skin patch for Parkinson's disease and moderate-to-severe primary restless legs syndrome that stimulates dopamine receptors in the brain. It is a less commonly prescribed cousin of oral dopamine agonists such as pramipexole, on the U.S. market since about 2012 and available only as the brand. Most people tolerate it reasonably well, though nausea, sleepiness, dizziness and an itchy, red patch site are the usual complaints. The one to take seriously is falling asleep without warning, even while driving and even months after starting. Report dizziness on standing, hallucinations or new urges to gamble or spend, and never stop it suddenly, since that can cause high fever and confusion.
Clinical pearls
- Put each new patch on a different spot (abdomen, thigh, hip, flank, shoulder or upper arm) and press firmly for 30 seconds.
- The patch contains sodium metabisulfite, so mention any sulfite sensitivity or asthma before starting it.
- Antipsychotics and metoclopramide (a nausea medicine) block dopamine and can weaken this patch, so tell every prescriber you use it.
- With heart failure or kidney problems, weigh yourself regularly and report new leg swelling or quick weight gain.
Patient information guide A plain-language walkthrough of Rotigotine Transdermal Patch, written from its FDA label.
What Rotigotine Transdermal Patch is used for
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Rotigotine patches, sold as Neupro, treat two conditions:
- Neupro is used for Parkinson's disease.
- Neupro is used for moderate-to-severe primary Restless Legs Syndrome.
How Rotigotine Transdermal Patch works
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Rotigotine is a non-ergoline dopamine agonist. It mimics dopamine by stimulating dopamine receptors in the brain.
In Parkinson's disease, this is thought to involve an area called the caudate-putamen. The exact way it helps Parkinson's disease and RLS is not known.
Rotigotine Transdermal Patch dosage
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Neupro is a patch worn on the skin and replaced once a day. You can use it with or without food.
- Apply to clean, dry, intact skin on the front of the abdomen, thigh, hip, flank, shoulder, or upper arm.
- Press firmly for 30 seconds, especially around the edges.
- Rotate sites daily. Don't reuse a site within 14 days.
- If the area is hairy, shave it at least 3 days before applying.
- If you forget to change the patch or it falls off, apply a new one for the rest of the day.
- Your dose may be made with one or more patches. To stop, your doctor will lower the dose gradually.
Dosing details from the FDA-approved label
From the Rotigotine Transdermal Patch prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Early-stage Parkinson's disease
- Initially 2 mg/24 hours
- May be increased weekly by 2 mg/24 hours if additional therapeutic effect is needed
- The lowest effective dose is 4 mg/24 hours
- Applied once a day
- Maximum: 6 mg/24 hours
- Advanced-stage Parkinson's disease
- Initially 4 mg/24 hours
- May be increased weekly by 2 mg/24 hours if additional therapeutic effect is needed
- Applied once a day
- Maximum: 8 mg/24 hours
- Restless Legs Syndrome
- Initially 1 mg/24 hours
- May be increased weekly by 1 mg/24 hours if additional therapeutic effect is needed
- The lowest effective dose is 1 mg/24 hours
- Applied once a day
- Maximum: 3 mg/24 hours
- Discontinuation in Parkinson's disease
- Reduce the daily dose by a maximum of 2 mg every 24 hours, preferably every other day, until complete withdrawal is achieved
- Discontinuation in Restless Legs Syndrome
- Reduce the daily dose by 1 mg every 24 hours, preferably every other day, until complete withdrawal is achieved
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION Parkinson's disease: Initially, 2 mg/24 hours for early-stage disease or 4 mg/24 hours for advanced-stage disease. The dose may be increased as needed by 2 mg/24 hours at weekly intervals, up to 6 mg/24 hours for early-stage disease and up to 8 mg/24 hours for advanced-stage disease. ( 2.1 ) Restless Legs Syndrome: Initially, 1 mg/24 hours, increased as needed by 1 mg/24 hours at weekly intervals, up to 3 mg/24 hours. ( 2.2 ) Apply once a day to the skin; press firmly in place for 30 seconds. Do not place NEUPRO on oily, irritated, or damaged skin, or where it will be rubbed by tight clothing. Do not use the same site more than once every 14 days. The prescribed dose may be achieved using single or multiple patches. ( 2.3 ) To discontinue treatment, reduce the dose gradually until complete withdrawal of NEUPRO. ( 2.4 ) 2.1 Dosage in Parkinson's Disease Early-Stage Parkinson's Disease In patients with early-stage Parkinson's disease, the recommended starting dose for NEUPRO is 2 mg/24 hours. Based upon individual patient clinical response and tolerability, NEUPRO dosage may be increased weekly by 2 mg/24 hours if additional therapeutic effect is needed. The lowest effective dose is 4 mg/24 hours. The maximum recommended dose for early-stage Parkinson's disease is 6 mg/24 hours. Advanced-Stage Parkinson's Disease In patients with advanced-stage Parkinson's disease, the recommended starting dose for NEUPRO is 4 mg/24 hours. Based upon individual patient clinical response and tolerability, NEUPRO dosage may be increased weekly by 2 mg/24 hours if additional therapeutic effect is needed. The maximum recommended dose for advanced-stage Parkinson's disease is 8 mg/24 hours. 2.2 Dosage in Restless Legs Syndrome In patients with Restless Legs Syndrome, the recommended starting dose for NEUPRO is 1 mg/24 hours. Based upon individual patient clinical response and tolerability, NEUPRO dosage may be increased weekly by 1 mg/24 hours if additional therapeutic effect is needed. The lowest effective dose is 1 mg/24 hours. The maximum recommended dose is 3 mg/24 hours. 2.3 Administration Information NEUPRO is applied once a day. The adhesive side of the transdermal system should be applied to clean, dry, intact healthy skin on the front of the abdomen, thigh, hip, flank, shoulder, or upper arm.
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Rotigotine Transdermal Patch side effects
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The most common side effects include:
Common side effects
- Skin reactions where the patch is applied
- Nausea
- Vomiting
- Sleepiness
- Dizziness
- Trouble falling or staying asleep
- Headache (especially in RLS)
- Swelling in the legs or feet (in Parkinson's disease)
- Sleep problems
- Loss of appetite, sweating, vision changes, and dyskinesia (uncontrolled movements) in Parkinson's disease
When to get medical help
- Call your doctor if you fall asleep during daily activities, including driving, or feel unusually sleepy. This can happen without warning.
- Call your doctor if you see or hear things that aren't there, or have new confusion, paranoia, or aggressive behavior.
- Get help if you feel faint, pass out, or get very dizzy when standing up.
- Tell your doctor about new, intense urges to gamble, spend money, binge eat, or have sex.
- Call your doctor about severe skin reactions at the patch site.
- Get emergency help for allergic-type reactions, such as wheezing or breathing trouble, especially if you are sensitive to sulfites.
- Do not stop the patch suddenly. Doing so can cause high fever and confusion.
Call your doctor about falling asleep suddenly, hallucinations, fainting, compulsive urges, or severe skin reactions.
Rotigotine Transdermal Patch warnings and precautions
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- Sudden sleep onset: some people fell asleep during daily activities, including driving, sometimes without warning.
- Hallucinations and psychosis: new or worse confusion, paranoia, or odd behavior can occur.
- Low blood pressure and fainting: most likely when starting or raising the dose.
- Compulsive behaviors: urges to gamble, spend, binge eat, or have sex.
- Higher blood pressure and heart rate in some people.
- Weight gain and swelling: especially in Parkinson's disease.
- Dyskinesia: Neupro can cause or worsen uncontrolled movements, especially with levodopa.
- Skin reactions: can be severe.
- Stopping suddenly: can cause high fever and confusion.
- Sulfite allergy: the patch contains sodium metabisulfite.
Rotigotine Transdermal Patch interactions
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Few interactions are listed for Neupro, but one matters:
- Antipsychotics and metoclopramide: these dopamine blockers may reduce how well Neupro works.
- Sedating medicines: your doctor should ask about these because they may raise the risk of drowsiness.
Interactions listed in the FDA-approved label
From the Rotigotine Transdermal Patch prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Dopamine antagonists, such as antipsychotics or metoclopramide: Dopamine antagonists may diminish the effectiveness of NEUPRO.
Read the label’s full interactions text
7 DRUG INTERACTIONS 7.1 Dopamine Antagonists Dopamine antagonists, such as antipsychotics or metoclopramide, may diminish the effectiveness of NEUPRO [see Clinical Pharmacology (12.3) ] .
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Rotigotine Transdermal Patch
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- Don't use it if you're allergic to rotigotine or any patch ingredient.
- Tell your doctor about sulfite sensitivity or asthma.
- Tell your doctor about psychotic disorders, heart disease, low blood pressure, or fainting.
- Heart failure or kidney problems call for monitoring of weight and swelling.
- Pregnancy: animal data show possible fetal harm; human data are lacking.
- Breastfeeding: it may reduce milk production, and effects on infants are unknown.
- Children: not established as safe or effective.
- Older adults: no overall differences were seen, but some may be more sensitive.
Rotigotine Transdermal Patch overdose
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Too much may cause nausea, vomiting, low blood pressure, involuntary movements, hallucinations, confusion, and convulsions. There is no known antidote. Remove extra patches right away and seek medical help, where heart rate, rhythm, and blood pressure are monitored.
What Rotigotine Transdermal Patch does in the body
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Rotigotine acts as a dopamine agonist. In a study at doses up to 24 mg/24 hours, it showed no sign of lengthening the QT interval, a measure of heart rhythm timing.
How your body processes Rotigotine Transdermal Patch
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After you apply the patch, the drug shows up in the blood after about 3 hours on average. Levels have no sharp peak, and steady levels are reached within 2 to 3 days. Where you place the patch can change how much is absorbed, with the shoulder absorbing more than the thigh in one study.
The body breaks rotigotine down into mostly inactive forms, and most leaves in the urine. After the patch is removed, levels fall with a half-life of 5 to 7 hours.
How to store Rotigotine Transdermal Patch
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Store at 20º - 25ºC (68º - 77ºF); excursions permitted between 15º - 30ºC (59º - 86ºF). stored in the original pouch. store outside of pouch.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Rotigotine Transdermal Patch
7 supplements and herbal products have documented interactions with Rotigotine Transdermal Patch in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Moderate · 6
- Minor · 1
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
Rotigotine Transdermal Patch: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Rotigotine Transdermal Patch — the kind of thing our pharmacy team would talk through with you at the counter.
What is this patch for?
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How do I put the patch on?
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What if I forget to change it or it falls off?
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Can I drive on this medicine?
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What side effects should I expect, and which ones need a call?
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Can I just stop using it if I feel better?
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Is Rotigotine Transdermal Patch available over the counter?
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When was Rotigotine Transdermal Patch first available?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Rotigotine Transdermal Patch on HelloPharmacist
Rotigotine Transdermal Patch forms and strengths (how it comes)
Rotigotine Transdermal Patch is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Need a version that does not list lactose, a gluten source, a dye or gelatin? Inactive ingredients differ by manufacturer: see Rotigotine Transdermal Patch inactive ingredients by manufacturer.
Skin patch
How this form is used
- Neupro is used to treat Parkinson's disease.
- Neupro is used to treat moderate-to-severe primary Restless Legs Syndrome.
- Neupro is applied once a day to clean, dry, healthy skin, at about the same time daily.
- Neupro should be pressed firmly in place for 30 seconds, and the site changed daily.
- Neupro should not go on oily, irritated, or damaged skin, or where tight clothing rubs.
- Neupro should not be applied to the same site more than once every 14 days.
Show 6 more strengths Show fewer strengths
Rotigotine Transdermal Patch on the U.S. market: products, makers and brands
How Rotigotine Transdermal Patch appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
1 company lists 6 Rotigotine Transdermal Patch product records with the FDA, mostly as skin patch; the earliest marketing or approval year on record is 2007. Brand names on the directory include Neupro; the rest are generics.
How widely Rotigotine Transdermal Patch is used (Medicaid data)
A general measure of how commonly Rotigotine Transdermal Patch is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Rotigotine Transdermal Patch is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Rotigotine Transdermal Patch prescribed? Of the 1,601 medications we measure, Rotigotine Transdermal Patch ranks #1,202 by Medicaid prescriptions — more than 25% of them.
Utilization by Rotigotine Transdermal Patch product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
24 HR rotigotine 0.0833 MG/HR Transdermal System Most dispensed
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 722253
24 HR rotigotine 0.167 MG/HR Transdermal System
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 722295
24 HR rotigotine 0.125 MG/HR Transdermal System
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1251916
24 HR rotigotine 0.0417 MG/HR Transdermal System
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1251912
24 HR rotigotine 0.25 MG/HR Transdermal System
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 722279
24 HR rotigotine 0.333 MG/HR Transdermal System
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1251920
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Rotigotine Transdermal Patch, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 6 of 12 listed Rotigotine Transdermal Patch NDCs with Medicaid activity.
Compare Rotigotine Transdermal Patch products
A representative set of FDA-listed product records for Rotigotine Transdermal Patch — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Skin patch | ||||
| ROTIGOTINE 1 mg/24h | Transdermal | UCB, Inc. | NDA | View NDC → |
| ROTIGOTINE 2 mg/24h | Transdermal | UCB, Inc. | NDA | View NDC → |
| ROTIGOTINE 3 mg/24h | Transdermal | UCB, Inc. | NDA | View NDC → |
| ROTIGOTINE 4 mg/24h | Transdermal | UCB, Inc. | NDA | View NDC → |
| ROTIGOTINE 6 mg/24h | Transdermal | UCB, Inc. | NDA | View NDC → |
| ROTIGOTINE 8 mg/24h | Transdermal | UCB, Inc. | NDA | View NDC → |
Showing 6 of 6 products — FDA National Drug Code Directory. See every product, package size and price: browse all 6 Rotigotine Transdermal Patch NDCs →
Rotigotine Transdermal Patch side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Rotigotine Transdermal Patch — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Rotigotine Transdermal Patch in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Rotigotine Transdermal Patch FDA approval history
How Rotigotine Transdermal Patch went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Rotigotine Transdermal Patch recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list no Rotigotine recalls since July 2021.
✅No Rotigotine recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 616739 1 dose form · 6 strengths
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Dose form (SCDF) Transdermal System RxCUI 1806004In current FDA listingsClinical drug / strength (SCD) 24 HR rotigotine 0.0417 MG/HRRxCUI 125191224 HR rotigotine 0.0833 MG/HRRxCUI 72225324 HR rotigotine 0.125 MG/HRRxCUI 125191624 HR rotigotine 0.167 MG/HRRxCUI 72229524 HR rotigotine 0.25 MG/HRRxCUI 72227924 HR rotigotine 0.333 MG/HRRxCUI 1251920
Look up RxCUI 616739 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Rotigotine Transdermal Patch supply and shortage status
Whether Rotigotine Transdermal Patch is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
💵 What Rotigotine Transdermal Patch costs pharmacies (NADAC benchmark)
The national average invoice price pharmacies pay for the drug itself, from CMS's NADAC survey (data as of Sep 30, 2026). This is a supply-cost benchmark — not a retail price and not what you'd pay at the counter.
| Form | Strength | Pharmacy acquisition benchmark | |
|---|---|---|---|
| Patch, Extended Release · Transdermal | ROTIGOTINE 1 mg/24h | $28.29 each | NDC details & price history |
| Patch, Extended Release · Transdermal | ROTIGOTINE 2 mg/24h | $28.26 each | NDC details & price history |
| Patch, Extended Release · Transdermal | ROTIGOTINE 3 mg/24h | $28.25 each | NDC details & price history |
| Patch, Extended Release · Transdermal | ROTIGOTINE 4 mg/24h | $28.32 each | NDC details & price history |
| Patch, Extended Release · Transdermal | ROTIGOTINE 6 mg/24h | $28.18 each | NDC details & price history |
| Patch, Extended Release · Transdermal | ROTIGOTINE 8 mg/24h | $28.24 each | NDC details & price history |
| Patch, Extended Release · Transdermal | 1 mg/24h | $28.29 each | NDC details & price history |
| Patch, Extended Release · Transdermal | 2 mg/24h | $28.26 each | NDC details & price history |
Source: CMS National Average Drug Acquisition Cost (NADAC), a survey of retail pharmacy invoice prices. Benchmarks shown are the range across package sizes of a representative product for each form and strength — other manufacturers' products may differ.
Rotigotine Transdermal Patch brand names
Rotigotine Transdermal Patch is sold under one brand name in the FDA directory — Neupro. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Rotigotine Transdermal Patch: manufacturers and labelers
One company lists Rotigotine Transdermal Patch products with the FDA. By number of product records, the largest are UCB, Inc.. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Rotigotine Transdermal Patch drug class (RxNorm)
Rotigotine Transdermal Patch belongs to the Nonergot Dopamine Agonist class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
Sources for this Rotigotine Transdermal Patch page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. UCB, Inc. is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →