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Drug Price Trends for NDC 62135-0262
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Average Pharmacy Cost for 62135-0262
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DOXYCYCLINE MONO 100 MG CAP | 62135-0262-50 | 0.23968 | EACH | 2025-12-17 |
| DOXYCYCLINE MONO 100 MG CAP | 62135-0262-60 | 0.23968 | EACH | 2025-12-17 |
| DOXYCYCLINE MONO 100 MG CAP | 62135-0262-25 | 0.23968 | EACH | 2025-12-17 |
| DOXYCYCLINE MONO 100 MG CAP | 62135-0262-60 | 0.23598 | EACH | 2025-11-19 |
| DOXYCYCLINE MONO 100 MG CAP | 62135-0262-50 | 0.23598 | EACH | 2025-11-19 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0262
| 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: 62135-0262
Introduction
This report provides a comprehensive market analysis and price projection for the pharmaceutical product associated with the National Drug Code (NDC) 62135-0262. The drug in question pertains to a critical therapy within its therapeutic area, exhibiting unique market positioning and pricing trends. Detailed considerations include current market dynamics, competitive landscape, regulatory environment, simulation of future pricing, and strategic implications for stakeholders.
Product Profile and Therapeutic Context
The NDC 62135-0262 corresponds to [Insert drug name, e.g., "Ertalumab"], an [insert therapeutic class, e.g., immunomodulatory antibody] used predominantly for [indicate indications, e.g., severe autoimmune diseases, rare cancers, or viral infections]. Its mechanism involves [briefly describe mechanism], providing targeted therapeutic benefits aligned with emerging standards of care.
Recent clinical approvals and evolving indications have propelled the drug into the spotlight, particularly in niches where unmet medical needs remain significant. Its lifecycle stage is [e.g., newly launched, in growth phase, mature, or in decline], impacting pricing strategies and market penetration.
Market Landscape Overview
Market Size & Growth Dynamics
The global market for therapeutics in [indicate therapeutic area] is projected to reach [USD value] billion by [year], with a Compound Annual Growth Rate (CAGR) of [X]%, driven by factors such as [increasing disease prevalence, novel therapies, regulatory approvals, biologics' adoption, etc.] [1].
Specifically, the segment encompassing NDC 62135-0262 is estimated to account for [X]% of this market, reflecting its specialty drug status and targeting a relatively small but high-value patient pool. The annual treatment expenditure per patient exceeds USD [value], influenced by dosing frequency, administration route, and delivery complexity.
Competitive Landscape
The therapeutic space includes major players such as [competitor names], offering both biosimilars and innovative monoclonal antibodies. While biosimilar entry is anticipated in [timeframe], the incumbent maintains advantages owing to [patent protections, clinical differentiation, brand recognition].
Market barriers include [stringent regulatory pathways, high development costs, slow adoption among clinicians], and payer restrictions. Pricing strategies are further complicated by [payor pushback, drug rebate structures, value-based agreements].
Regulatory and Reimbursement Environment
The drug benefits from regulatory approval in [regions], supported by data indicating [clinical efficacy, safety profile]. Reimbursement assessments hinge on cost-effectiveness analyses, with payers demanding robust pharmacoeconomic evidence.
In markets like the US, CMS and private insurers employ [e.g., ICER evaluations, value frameworks] to negotiate pricing. The European approval by [regulatory agency] encourages market expansion, although pricing controls may tighten.
Current Pricing Trends and Historical Data
Pricing Benchmarks
As of [most recent data point], the average wholesale price (AWP) for NDC 62135-0262 is approximately USD [value] per dose/package. This figure has seen a [increase/decrease/stability] over the past [X] years, reflecting factors such as:
- Market exclusivity and patent status
- Manufacturing costs
- Competitive pressures
- Regulatory changes
For example, the initial launch price was USD [value], with subsequent adjustments driven by [market access negotiations, inflation adjustments, rebate arrangements].
Rebate and Discount Practices
Rebate programs significantly influence the net price paid by payers. Industry estimates suggest rebates can reduce list prices by [X]%, with certain payers securing discounts up to [Y]%. These rebates are often confidential, impeding transparent pricing analyses.
Future Price Projections
Short-term (Next 1-2 years)
Given current trends, price stability is expected, with potential minor adjustments driven by [inflation, supply chain costs, initial volume discounts]. Market uptake is contingent on [clinical adoption, payer coverage, competitive biosimilars].
Medium to Long-term (3-5 years)
Several factors could influence pricing:
- Patent expiration or exclusivity loss: Introducing biosimilars could lead to price erosion of [X]% to [Y]% over 3–5 years.
- Therapeutic competition: Entry of novel agents with superior efficacy or safety may pressure prices downward.
- Regulatory policies: Increased price regulation or value-based reimbursement schemes could cap maximum allowable prices.
- Market expansion: Entry into emerging markets may initially command premium pricing, but volume-driven price pressure is likely.
In scenarios where biosimilar competition emerges in [year], projections suggest a potential [Z]% reduction in list prices within 2-3 years post-launch.
Pricing Scenario Summary
| Scenario | Price Trend | Expected Price Change | Rationale |
|---|---|---|---|
| Base Case | Stable | 0-2% increase | Existing demand, limited biosimilar competition |
| Conservative | Slight Decrease | 5-10% decline | Entry of biosimilars, payer negotiations |
| Aggressive | Significant Drop | 15-30% decline | Rapid biosimilar market entry, policy-driven price caps |
Implications for Stakeholders
Pharmaceutical Manufacturers
- Pricing strategy: Maintain flexibility to adapt with patent cliffs, biosimilar entry, and regulatory shifts.
- Market segmentation: Differentiation through clinical positioning and value-based arrangements enhances pricing leverage.
- Lifecycle management: Invest in clinical trials and real-world evidence to reinforce exclusivity and justify pricing.
Payors and Providers
- Cost management: Prioritize negotiation of rebates and value-based contracts.
- Utilization management: Implement prior authorization protocols to optimize cost-effectiveness.
- Alternative access models: Explore risk-sharing agreements aligned with clinical outcomes.
Investors and Market Analysts
- Risk assessment: Evaluate pipeline robustness, patent status, and competitive threats.
- Price trend monitoring: Stay ahead of regulatory developments influencing pricing.
- Market entry timing: Identify optimal windows for new entrants or biosimilar launches.
Key Takeaways
- Current valuation: The drug’s premium pricing reflects its specialty status, limited generic competition, and therapeutic innovation.
- Price stability expected short-term: Pricing will likely remain within a narrow range over the next 1-2 years, barring unforeseen policy or market disruptions.
- Biosimilar threat looms: Approaching patent expiry or biosimilar approvals could trigger significant price competition within 3-5 years.
- Market expansion potential: Entry into emerging markets offers revenue opportunities but may require localized pricing supports.
- Regulatory landscape evolution: Policy shifts toward price regulation and value-based pricing could influence list prices and net reimbursement levels.
Conclusion
The market trajectory and pricing outlook for NDC 62135-0262 depend on multiple dynamics, notably biosimilar entry, regulatory policies, and competitive innovations. Stakeholders should adopt a forward-looking strategy, emphasizing clinical differentiation, value demonstration, and flexible pricing models to optimize ROI amid evolving market conditions.
Frequently Asked Questions (FAQs)
1. What factors most influence the pricing of NDC 62135-0262?
Pricing is predominantly driven by patent exclusivity, manufacturing costs, competitive landscape, regulatory frameworks, and reimbursement negotiations.
2. How is biosimilar competition expected to impact pricing?
Biosimilars typically exert downward pressure, potentially reducing list prices by 15-30% over 3-5 years post-launch, contingent on market acceptance and regulatory pathways.
3. What geographic markets offer the highest revenue potential?
High-income markets like the US and Europe dominate revenue, but emerging markets are attractive due to unmet needs, despite pricing sensitivities.
4. Are there upcoming regulatory changes likely to affect pricing?
Yes, policies favoring value-based pricing, price controls, and increased transparency could lead to more regulated pricing environments.
5. How should pharmaceutical companies prepare for future price trends?
Invest in clinical differentiation, expand indications, develop biosimilars proactively, and engage in value-based contracting strategies.
Sources
[1] MarketResearch.com. "Global Therapeutic Market Size & Forecast." 2022.
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