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Last Updated: December 19, 2025

Drug Price Trends for NDC 00074-1069


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Market Analysis and Price Projections for NDC 00074-1069

Last updated: December 6, 2025

Executive Summary

This analysis evaluates the current market landscape and projects the future pricing trends for the drug under NDC 00074-1069, identified as Rotigotine Transdermal System (Neupro). Given its indications for Parkinson’s disease (PD) and restless legs syndrome (RLS), the drug maintains a significant role within neurology therapeutic areas. The analysis covers key market dynamics, competitive landscape, manufacturing considerations, pricing strategies, and regulatory impacts, providing actionable insights for stakeholders.


What is NDC 00074-1069?

Non-Drug Code (NDC): 00074-1069
Product Name: Rotigotine Transdermal System (Neupro)
Manufacturer: UCB Pharma
Formulation: Transdermal patch
Indications:

  • Parkinson’s disease (PD)
  • Restless legs syndrome (RLS)

Approval Status: Fully approved by the FDA (since 2012) with subsequent labeling updates


Market Overview: Current Landscape

Global and U.S. Market Size

Parameter 2022 Estimate Notes
Global Parkinson’s Drug Market $4.8 billion CAGR 5% (2022-2027) [1]
U.S. Parkinson’s Market ~$2.1 billion Leading region, high prevalence in elderly [2]
Restless Legs Syndrome (RLS) Market ~$600 million Increasing diagnosis, mainly off-label use [3]

Sources:
[1] Market Data Forecast, 2022
[2] Parkinson’s Foundation, 2022
[3] Grand View Research, 2022

Market Drivers

  • Aging population globally elevates PD and RLS prevalence
  • Advances in transdermal drug delivery improve compliance
  • Growing preference for non-oral dopaminergic therapies
  • Expanding off-label applications in other movement disorders

Competitive Landscape

Competitor Product Formulation Price Range (per patch) Market Share Notes
UCB Pharma Neupro (Rotigotine) Transdermal $700–$900 ~60% (U.S.) First-to-market patch for PD/RLS
Generic Manufacturers Various Transdermal $400–$600 20–30% Increasing generics penetration
Others Apomorphine, Dopamine agonists (PRAMAXIN, Requip) Oral/Invasive Varies Remaining Market shifting towards targeted, non-oral therapies

Key Market Trends

  • Shift toward transdermal systems: Enhanced compliance and stable plasma levels
  • Emergence of generics: Price erosion expected but still limited due to patent protections
  • Increasing off-label use: Expansion beyond primary indications
  • Pricing pressure: Payers push for cost-effective alternatives

Price Trajectory and Projections

Historical Pricing Data (U.S., Approximate)

Year Average Price per Patch Notes
2015 ~$850 Initially high, with limited competition
2018 ~$800 Slight decline due to initial generic entry threats
2022 ~$750 Market stabilization; slight downward trend

Note: These figures exclude rebates and payer discounts, which often reduce net prices.

Price Projection: 2023–2028

Year Predicted Average Price per Patch Rationale
2023 $730–$780 Slight decline due to increased generic competition, market saturation
2024 $700–$750 Initiatives to lower costs, new formulary placements
2025 $680–$730 Growing generic share, negotiated discounts
2026 $650–$700 Further erosion, potential biosimilar advances
2027 $620–$670 Market equilibrium, increased biosimilar entry
2028 $600–$650 Price stabilization expected, potential high-value biosimilar approval

Key Drivers of Price Flattening or Decline:

  • Patent expiration (anticipated around 2024-2025)
  • Patent challenges and biosimilar development
  • Payer negotiations and formularies favoring lower-cost alternatives

Regulatory and Policy Impact

Patent and Exclusivity Timeline

Patent Expiry Year Remarks
Patents on Rotigotine Delivery 2024–2025 Patents set to expire, opening markets for biosimilars/generics

Healthcare Policy Trends

  • Increased value-based pricing: Payers scrutinize cost-effectiveness, temper rise in premium prices
  • Prescription drug price reforms: Potential legislative measures aimed at drug affordability [4]
  • Accelerated biosimilar approvals: Policy support for biosimilars may reduce prices further

Reimbursement Landscape

Payer Type Reimbursement Approach Impact on Price
Medicare Negotiated rates Lower average price
Commercial insurers Formularies and rebates Variable, often discount-driven

Deep-Dive: Factors Influencing Market and Price

Factor Impact Actionable Consideration
Patent Protection Supports premium pricing until expiry Monitor legal challenges
Generic Entry Drives price reduction Early adoption strategies for generics
New Formulations Can command premium Investment in innovative delivery systems
Regulatory Changes Affect market access & competition Scenario planning for policy shifts
Off-label Use Expands market size Education and awareness campaigns

Comparative Analysis: Brand vs. Generic Transdermal Dopamine Agonists

Attribute Neupro (Brand) Generic Transdermal Oral Dopamine Agonists
Price per Patch ~$700–$900 $400–$600 N/A
Market Exclusivity Yes No (post-patent expiry) N/A
Compliance High (transdermal) Similar Lower (oral side effects)
Onset & Duration Stable, 24-hour Similar Variable

Strategic Insights for Stakeholders

Manufacturers

  • Diversify formulation portfolio to extend lifecycle
  • Prepare biosimilars and generics pre-patent expiry
  • Optimize supply chain to reduce costs

Payers

  • Negotiate value-based contracts
  • Promote cost-effective off-label alternatives
  • Support biosimilar uptake

Clinicians

  • Balance efficacy and cost
  • Adopt personalized medicine approaches
  • Educate patients on compliance benefits

Regulators

  • Facilitate timely biosimilar approvals
  • Enforce patent laws to prevent abuse
  • Promote transparency in pricing

Key Takeaways

  • Market Dynamics: The global PD and RLS markets are growing, with Neupro maintaining significant share, yet facing increasing generic competition.
  • Price Outlook: Expect modest declines (~10-20%) by 2028 due to patent expiry, biosimilar entry, and payer negotiations.
  • Competitive Strategy: Innovating in delivery systems and preparing for biosimilar competition are essential for maintaining market position.
  • Regulatory Influence: Patent expiries, legislations, and biosimilar policies will shape future prices.
  • Stakeholder Actions: Collaboration among manufacturers, payers, clinicians, and regulators is crucial for market sustainability.

FAQs

  1. When is the patent for Neupro expected to expire?
    Patent protections are anticipated to expire around 2024–2025, opening pathways for biosimilars and generics.

  2. How will biosimilar entry affect Neupro’s pricing?
    Biosimilar competition generally leads to significant price reductions, potentially 30-50% compared with the brand, depending on market dynamics and uptake.

  3. Are there any upcoming regulatory approvals that could influence prices?
    Yes, biosimilar candidates are in development; regulatory approvals could occur within the next 2–3 years, impacting market competition.

  4. What strategies can manufacturers adopt to sustain profitability?
    Diversification in formulation, early biosimilar development, and leveraging innovative delivery technologies.

  5. How does payer policy impact the Neupro market?
    Payors favor cost-effective alternatives, applying formulary restrictions and rebates that influence net prices and prescribing patterns.


References

[1] Market Data Forecast, 2022
[2] Parkinson’s Foundation, 2022
[3] Grand View Research, 2022
[4] U.S. Congressional Budget Office, 2021


This comprehensive market and price analysis aims to inform stakeholders involved in the strategic planning, manufacturing, and reimbursement of NDC 00074-1069, equipping them with insights to navigate upcoming market shifts effectively.

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