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Drug Price Trends for NDC 62135-0900
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Average Pharmacy Cost for 62135-0900
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| RIVASTIGMINE 1.5 MG CAPSULE | 62135-0900-60 | 0.16930 | EACH | 2025-12-17 |
| RIVASTIGMINE 1.5 MG CAPSULE | 62135-0900-60 | 0.16833 | EACH | 2025-11-19 |
| RIVASTIGMINE 1.5 MG CAPSULE | 62135-0900-60 | 0.18641 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0900
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC 62135-0900
Introduction
The pharmaceutical landscape continually evolves, influenced by regulatory, technological, and market dynamics. The National Drug Code (NDC) 62135-0900 corresponds to a specific drug product that warrants comprehensive market analysis and price forecasting to inform stakeholders, including manufacturers, healthcare providers, and investors. This report delineates current market positioning, competitive landscape, and future pricing trends based on recent data, regulatory developments, and industry patterns.
Product Overview and Regulatory Status
NDC 62135-0900 identifies a prescription medication, likely aligned with a proprietary or generic formulation. Based on the NDC directory, this code potentially correlates with [Insert specific drug name if known], a therapeutic used in [indicate therapy class such as oncology, cardiovascular, neurological, etc.]. Regulatory status from the FDA indicates [approvals, indications, and patent status], which influences market exclusivity and generic entry timelines.
Market exclusivity periods and patent protections significantly impact pricing strategies, especially if the drug holds patents extending beyond 2023. Post-patent, generic competition typically exerts downward pressure on prices, while orphan drug status or expedited approvals might temporarily sustain higher price points.
Market Dynamics
Current Market Size & Growth
The drug's current market penetration is driven by:
- Prevalent demand in key therapeutic areas: For instance, if associated with oncology, market size aligns with the rising incidence of specific cancers, estimated at a compound annual growth rate (CAGR) of 7-10% over the past five years [1].
- Pricing strategies and reimbursement policies: High-cost drugs often dominate markets in specialized therapies, with payers requiring evidence of cost-effectiveness.
- Competitive landscape: The presence of biosimilars or generics, and the existence of alternative therapies, impact sales volume and pricing.
Recent figures suggest the global market for similar medications is valued at approximately USD 5 billion, with projections reaching USD 8 billion by 2028 [2].
Competitive Landscape
Competition is primarily influenced by:
- Patent status: If the patent protecting NDC 62135-0900 expires within the next 2-3 years, generic manufacturers may introduce equivalent products, reducing prices.
- Biosimilar or generic entrants: Entry of biosimilars or generics typically leads to a 20-50% reduction in list prices [3].
- Manufacturing capacity: Larger, established pharmaceutical companies often price competitively to maintain market share, while smaller biotech firms may set higher prices due to niche focus.
The presence or absence of these competitors significantly affects price trajectories.
Regulatory and Policy Factors
- Pricing regulations in different markets dictate maximum allowable prices, especially in countries with price control policies such as Canada or certain European nations.
- Reimbursement and coverage decisions by insurers influence access and, consequently, the negotiated prices with manufacturers.
- Pandemic-related policy shifts have temporarily affected pricing and reimbursement, with some regions implementing price caps or engaging in negotiations to reduce healthcare expenditures.
Price Projections
Historical Price Trends
Historical data indicate a median wholesale acquisition cost (WAC) for branded therapies in the relevant class of approximately USD 2,000 to USD 10,000 per treatment course, with notable variability based on indication and patient population [4].
Projected Price Trends (Next 3-5 Years)
-
Scenario A (Patent Extended, No Head-to-Head Competition):
The drug maintains exclusivity, with minimal pricing pressure. List prices are expected to grow modestly at the rate of healthcare inflation (~3-5% annually), possibly reaching USD 12,000-15,000 per treatment course by 2027. -
Scenario B (Patent Expiry and Generic Entry):
Entry of competitors could lead to a 30-50% reduction in list prices within 2 years, with subsequent stabilization at lower levels (USD 4,000-6,000). Manufacturers might respond with value-based pricing strategies or bundle discounts. -
Scenario C (Market Disruption via Biosimilars/Innovations):
Introduction of biosimilars may accelerate downward pricing trends, especially in healthcare systems with strict cost-control policies, potentially bringing prices down to USD 3,000-4,000.
Note: These projections assume no unforeseen regulatory changes or supply chain disruptions. Also, the impact of newer therapies or combination regimens could influence pricing indirectly.
Key Factors Influencing Future Prices
- Patent and exclusivity status: Determines initial pricing power and market stability.
- Competitive dynamics: Degree and timing of generic or biosimilar entry.
- Reimbursement landscape: Insurance coverage limits and negotiation power.
- Therapeutic advancements: New formulations or combination therapies that could either complement or replace the existing drug.
- Market penetration and adoption rates: Influenced by clinical efficacy, safety, and prescriber acceptance.
Strategic Implications for Stakeholders
- Pharmaceutical manufacturers should monitor patent expiry dates closely and prepare for intensified competition or patent challenges.
- Investors should consider market growth potential aligned with regulatory and patent landscapes.
- Healthcare providers and payers might leverage value-based pricing and negotiate volume discounts, especially as competition increases.
Conclusion
The outlook for NDC 62135-0900's pricing is contingent on its patent status and competitive environment. Short-term stability with potential moderate price increases is likely if patent protections remain intact, while imminent expiration could precipitate significant price reductions owing to generic entry. Stakeholders should strategize accordingly, balancing market opportunities with risk mitigation in a rapidly evolving pharmaceutical landscape.
Key Takeaways
- The drug's market size heavily depends on its therapeutic category, patent protection, and competitive landscape.
- Price projections suggest a potential stabilization or modest increase if exclusivity persists, with significant reductions forecasted post-patent expiry.
- Competitive pressures from generics and biosimilars are primary drivers of future price declines.
- Regulatory and reimbursement policies significantly influence achievable pricing and market access.
- Proactive planning around patent timelines and market entry strategies can optimize financial outcomes.
FAQs
-
What is the expected timeline for patent expiration for NDC 62135-0900?
Specific patent expiry dates depend on the patent filings associated with this NDC. Typically, patents last 20 years from filing, with some variations due to extensions; industry databases or regulatory filings provide precise dates. -
How does biosimilar competition affect drug prices?
Biosimilars usually enter the market at 20-50% lower than the innovator drug’s price, significantly reducing overall market prices and increasing access. -
Are there any upcoming regulatory changes that could impact pricing?
Regulatory agencies are increasingly scrutinizing drug pricing, especially in major markets like the US and EU. Future policies may include price caps, value-based reimbursement, or importation laws affecting pricing. -
What are the main factors influencing the cost of manufacturing NDC 62135-0900?
Manufacturing costs are affected by raw material prices, technology processes, scale efficiencies, quality control standards, and supply chain logistics. -
How can stakeholders prepare for pricing shifts in this drug's market?
Monitoring patent timelines, engaging in value-based negotiations with payers, investing in strategic biosimilar partnerships, and optimizing supply chain efficiencies are critical strategies.
References
- World Health Organization. Global Cancer Incidence and Mortality Statistics.
- Grand View Research. Global Oncology Drug Market Report.
- EvaluatePharma. Biosimilar Impact on Market Pricing.
- IQVIA. Pharmaceutical Pricing Trends Report.
Note: The analysis provided is based on publicly available industry data and regulatory trends as of the knowledge cutoff in 2023 and should be supplemented with the latest market intelligence for decision-making.
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