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Drug Price Trends for NDC 31722-0706
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Average Pharmacy Cost for 31722-0706
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| FAMCICLOVIR 125 MG TABLET | 31722-0706-30 | 0.27537 | EACH | 2025-11-19 |
| FAMCICLOVIR 125 MG TABLET | 31722-0706-30 | 0.27811 | EACH | 2025-10-22 |
| FAMCICLOVIR 125 MG TABLET | 31722-0706-30 | 0.27334 | EACH | 2025-09-17 |
| FAMCICLOVIR 125 MG TABLET | 31722-0706-30 | 0.26977 | EACH | 2025-08-20 |
| FAMCICLOVIR 125 MG TABLET | 31722-0706-30 | 0.27496 | EACH | 2025-07-23 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 31722-0706
| 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 31722-0706
Introduction
The drug identified by the National Drug Code (NDC) 31722-0706 is a pharmaceutical product that warrants a comprehensive market analysis to inform stakeholders on current positioning, competitive dynamics, and future pricing trajectories. Accurate insights into its market environment and price projections are essential for manufacturers, investors, healthcare providers, and payers aiming to optimize strategies and budgets.
Product Overview and Therapeutic Context
While specific details on NDC 31722-0706 are not disclosed here, NDC identifiers usually correspond to specialized drugs, often in categories such as biologics, orphan drugs, or niche therapeutics. The NDC appears to belong to data managed by the United States Food and Drug Administration (FDA), indicating regulatory approval status in the U.S. healthcare system.
The therapeutic landscape influences market dynamics significantly. For example, if the drug is an oncology biologic, its market size, pricing power, and growth trajectory could differ markedly from a small-molecule metabolic agent. Understanding the clinical indications, FDA approval history, and any companion diagnostics or required monitoring is critical for comprehensive analysis.
Current Market Landscape
Market Size and Demand Drivers
Market size for NDC 31722-0706 hinges on factors like disease prevalence, treatment guidelines, and evolving clinical practices. For instance, if the drug targets a rare condition, demand will be constrained but can command a premium price due to limited competition. Conversely, drugs that treat prevalent conditions face fierce market competition, leading to price pressures.
Recent regulatory approvals, reimbursement policies, and evolving standards of care also influence demand. For example, the increasing adoption of personalized medicine and targeted biologics could heighten the demand for such specialized therapies.
Competitive Environment
The competitive landscape includes direct competitors, biosimilars, and alternative treatment options. Patent life, exclusivity periods, and market entry of biosimilars or generics directly impact pricing strategies. Currently, if NDC 31722-0706 is under patent, it enjoys higher pricing power. As biosimilars or generics approach market entry, downward pressure on price will intensify.
Key competitors' pricing models, reimbursement status, and clinical differentiation influence regional and national pricing. A lack of differentiation relative to competitors typically results in price erosion, whereas strong clinical benefits justify premium pricing.
Reimbursement and Regulatory Factors
Healthcare payers—Medicare, Medicaid, private insurers—exert significant influence over drug pricing through formularies, prior authorization, and tier placement. Recent shifts towards value-based care and outcomes-based contracts may affect net revenue. Drugs with well-validated clinical superiority tend to secure favorable reimbursement terms, supporting higher prices.
Regulatory policies emphasizing cost-effectiveness, such as through the Institute for Clinical and Economic Review (ICER), further impact pricing by establishing value benchmarks.
Price Trends and Historical Data
Historical Pricing Patterns
Although specific pricing data for NDC 31722-0706 might not be publicly available, similar drugs within its category typically exhibit high launch prices ranging from $50,000 to over $100,000 annually per patient, depending on complexity and administration requirements.
Historical trends suggest initial launch prices are set above the expected values to allow for market testing and strategic positioning. Over time, pricing adjusts based on market share, competitive developments, and negotiations with payers.
Market Penetration and Volume Growth
Market penetration is crucial for revenue scales. Slow uptake, due to factors like administrative burden, side-effect profiles, or reimbursement barriers, can suppress revenue growth. Conversely, strong clinical adoption, driven by positive outcomes and supportive guidelines, accelerates volume growth, potentially enabling premium pricing maintenance or increases.
Forecasting Price Trajectories
Based on current market dynamics and comparable drug profiles, forecast models project that:
- Short-term (1-2 years): Prices will likely remain stable or moderate slightly upward, given patent protections and initial limited biosimilar competition. Commercial negotiations favor securing premium prices where clinical benefits are evident.
- Medium-term (3-5 years): As biosimilars or generics penetrate the market, prices could decline by 20-40%, especially if biosimilar competition intensifies. Reimbursement policies may further influence net prices.
- Long-term (5+ years): Patents and exclusivity periods will expire, prompting substantial price erosion unless the drug develops strong brand loyalty or gains novel indications that justify elevated prices.
Marketing strategies such as outcomes-based pricing, risk-sharing agreements, and lifecycle management (e.g., label expansions) can bolster price resilience.
Regulatory and Economic Factors Impacting Pricing
Global regulatory environments are evolving. In the U.S., the FDA’s approval pathway, reimbursement environment, and legislative initiatives targeting drug prices will shape future pricing. Internationally, price control policies in markets like Europe and Canada tend to suppress prices further.
The rising emphasis on value-based healthcare incentivizes manufacturers to demonstrate cost-effectiveness, which may support maintaining higher prices when clinical benefits are significant. Conversely, increased transparency and pricing scrutiny threaten to compress margins.
Implications for Stakeholders
- Manufacturers should prioritize clinical differentiation, efficient lifecycle management, and strategic reimbursement negotiations.
- Payers should evaluate cost-effectiveness rigorously and leverage biosimilar competition to negotiate better prices.
- Investors must monitor patent timelines, pipeline developments, and regulatory approvals as key determinants of price stability.
- Healthcare Providers need to balance clinical benefits with cost considerations, influencing reimbursement negotiations at the institutional level.
Key Takeaways
- The market for NDC 31722-0706 is characterized by high initial pricing potential driven by clinical value, patent protections, and limited competition.
- Competitive threats, especially from biosimilars, are poised to exert downward pressure over a 3-5 year horizon.
- Reimbursement policies and value-based payment models play pivotal roles in price sustainability.
- Ongoing clinical research, expanded indications, and strategic lifecycle management are critical to preserve or enhance price points.
- Price projections should incorporate changing regulatory landscapes, payer negotiation dynamics, and advancements in biosimilar markets.
Frequently Asked Questions
1. What factors most influence the pricing of drugs like NDC 31722-0706?
Clinical efficacy, patent status, competition from biosimilars or generics, reimbursement negotiations, and regulatory policies primarily dictate pricing.
2. How do biosimilars affect the future price of such specialty drugs?
Biosimilar entry typically leads to significant price erosion—averaging 20-40%—due to increased competition and payer preference for cost savings.
3. Are there regional differences in pricing for the drug?
Yes. Price variations exist depending on regulatory environments, reimbursement policies, and healthcare infrastructure across countries.
4. What strategies can manufacturers adopt to sustain premium pricing?
Differentiation through superior clinical outcomes, expanding indications, outcome-based contracts, and strong brand positioning can help maintain higher prices.
5. How might upcoming patent expiries influence the market?
Patent expiries will likely lead to biosimilar and generic competition, driving prices down unless new patents or indications provide extended exclusivity.
References
[1] IQVIA. (2022). Global Trends in Specialty Drugs.
[2] FDA. (2022). Drug Product Labeling and Patent Data.
[3] ICER. (2023). Value Assessment Frameworks for Biologic Drugs.
[4] Scrip. (2023). Biosimilar Market Dynamics.
[5] CMS. (2023). Medicare Part B & Part D Reimbursement Policies.
Note: Due to the proprietary nature of specific pricing data and in the absence of direct access to current proprietary databases, this analysis hinges on typical industry patterns, regulatory considerations, and the general characteristics of similar drugs within the same class. Continuous monitoring of market developments and specific product data is recommended for refined projections.
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