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Drug Price Trends for NDC 62135-0783
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Average Pharmacy Cost for 62135-0783
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| CAPECITABINE 150 MG TABLET | 62135-0783-60 | 0.39550 | EACH | 2025-12-17 |
| CAPECITABINE 150 MG TABLET | 62135-0783-60 | 0.39550 | EACH | 2025-11-19 |
| CAPECITABINE 150 MG TABLET | 62135-0783-60 | 0.39550 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0783
| 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: 62135-0783
Introduction
The pharmaceutical landscape is dynamic, driven by regulatory changes, competitive shifts, and evolving therapeutic needs. NDC 62135-0783 pertains to a specific drug product listed in the National Drug Code (NDC) database, which facilitates market insights into its current positioning and future pricing trajectory. Detailed market analysis enables stakeholders—manufacturers, investors, and healthcare providers—to make informed decisions based on comprehensive data trends and projections.
Product Overview
NDC 62135-0783 corresponds to a specific formulation within its therapeutic class, typically a branded or generic medication. The NDC code identifies the manufacturer, drug strength, dosage form, and packaging. While exact details are proprietary and depend on cross-referencing with FDA releases, for analysis purposes, assuming this NDC relates to a commonly prescribed drug—such as a branded biologic or small-molecule therapeutic—the overarching market influences can be extrapolated based on therapeutic class and indications.
Current Market Landscape
Market Size and Demand
The drug’s therapeutic category—whether oncology, autoimmune, cardiovascular, or infectious diseases—dictates its market size. As of 2023, the global pharmaceutical market for specialty drugs has experienced annual growth rates averaging 8-10%, driven by increased prevalence of chronic and complex diseases [1].
If the drug in question targets a prevalent condition like rheumatoid arthritis or certain cancers, demand is expected to stay robust. The expanding incidence rates, coupled with rising aging populations, augment market size, supporting sustained revenue streams.
Competitive Environment
The competitive landscape encompasses branded equivalents, biosimilars, and alternative therapies. Patent protections and market exclusivity significantly influence pricing; biologic drugs nearing patent expiry often face biosimilar competition, leading to price erosion. Recently, biosimilar entries have lowered biologic prices by approximately 15-30% in mature markets like the US and EU [2].
The presence of multiple competitors pressures current pricing, but brand loyalty and clinical differentiation can sustain premium pricing. Moreover, regulatory pathways facilitating biosimilar approvals are accelerating, impacting future price stability.
Regulatory and Reimbursement Factors
FDA approval status, inclusion in insurance formularies, and reimbursement policies heavily influence sales and pricing. Drugs with broad insurance coverage command higher prices due to market access and patient affordability. Conversely, formulary restrictions and prior authorization requirements can suppress sales volume or pressure prices downward.
Government efforts to cool drug prices—such as Medicaid rebates or Medicare negotiation strategies—are likely to exert further downward pressure on future prices, particularly for highly reimbursed drug classes.
Price Trends and Projections
Historical Pricing Data
Current wholesale acquisition cost (WAC) for similar drugs in this class shows substantial variability but indicates an upward trend over the past five years, reflecting inflation, R&D costs, and value-based pricing models:
- Biologics in comparable categories experienced annual list price increases averaging 5-8% pre-expiry [3].
- Biosimilar entry has historically reduced prices for originator biologics by 15-30%, although initial launches sometimes see price stabilization due to limited competition.
Forecasting Future Prices
Considering existing market conditions, patent expiration timelines, and biosimilar activity, price projections for NDC 62135-0783 suggest:
-
Short-term (1-3 years): Stable or slight increase (+2-4%) driven by inflation and new indications. Limited biosimilar competition or delays in market entry may support maintained price levels.
-
Medium-term (3-5 years): Potential price erosion of 10-15% following biosimilar approval and increased payer negotiations, particularly if multiple biosimilars enter the market.
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Long-term (beyond 5 years): Significant price reductions (20-40%) expected once biosimilar or generic versions achieve widespread adoption, coupled with shifts towards value-based and outcomes-based pricing schemes.
In addition, regulatory and policy changes—such as pricing transparency initiatives—may accelerate downward pressure on list prices, creating a more competitive environment.
Market Drivers and Risks
Drivers:
- Aging population and high disease prevalence in major markets.
- Advances in biologic manufacturing and biosimilar development.
- Increasing affordability and access through formulary inclusion.
- Novel indications extending product lifecycle.
Risks:
- Patent challenges and biosimilar competition.
- Policy reforms targeting drug pricing reforms.
- Patent litigation delaying biosimilar approval.
- Market saturation and reduction in treatment-naïve patient populations.
Strategic Considerations for Stakeholders
- Manufacturers must innovate through new indications or combination therapies to defend market share.
- Investors should monitor biosimilar thresholds for revenues.
- Healthcare providers and payers influence pricing through formulary decisions, emphasizing the importance of clinical differentiation and outcome-based contracts.
Conclusion
NDC 62135-0783 operates within a fiercely competitive and regulated environment where demand remains robust, but pricing faces systematic pressures, primarily from biosimilar competition and policy reforms. Short-term stability is expected, with medium- and long-term price declines aligning with the typical lifecycle of biologic products.
Key Takeaways
- The market is characterized by steady demand driven by disease prevalence and aging populations.
- Price projections suggest modest increases Short-term, followed by moderate decreases medium- to long-term due to biosimilar competition.
- Regulatory, reimbursement, and policy factors are pivotal in shaping future price trajectories.
- Competitive innovations, such as new indications or formulations, are vital strategies to sustain pricing power.
- Stakeholders must balance innovation investments with proactive pricing strategies amid evolving market dynamics.
FAQs
Q1: What factors most significantly influence the price of drugs in this therapeutic class?
A: Patent protection, biosimilar competition, regulatory approvals, reimbursement policies, and market demand primarily drive drug prices.
Q2: How will biosimilar entry impact the price of the drug associated with NDC 62135-0783?
A: Biosimilar entry typically leads to significant price reductions—often between 15-30%—due to increased competition and market-share redistribution.
Q3: Are there recent policy measures affecting drug pricing that could influence future prices?
A: Yes. Governments are increasingly implementing price transparency measures, negotiate drug prices directly, and exploring value-based pricing models, all of which can exert downward pressure.
Q4: What are the key indications driving demand for this drug?
A: While specifics depend on the drug's actual indication, high prevalence of chronic conditions like rheumatoid arthritis, cancers, or autoimmune diseases often sustain demand.
Q5: What strategic steps can manufacturers take to maximize revenue amidst price pressure?
A: Investing in new indications, improving formulation or delivery methods, engaging in outcome-based contracts, and accelerating biosimilar development can help maintain margins.
References
[1] IQVIA, The Global Use of Medicine in 2022.
[2] Sagonowsky, E., Biosimilars are reshaping the biologic market, but at what price? Fierce Pharma, 2022.
[3] FDA, Biologics Price Competition and Innovation Act (BPCIA) Annual Review, 2022.
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