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Drug Price Trends for NDC 71699-0100
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Average Pharmacy Cost for 71699-0100
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| XCOPRI 100 MG TABLET | 71699-0100-30 | 38.77292 | EACH | 2025-11-19 |
| XCOPRI 100 MG TABLET | 71699-0100-30 | 38.77288 | EACH | 2025-10-22 |
| XCOPRI 100 MG TABLET | 71699-0100-30 | 38.78946 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 71699-0100
| 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 71699-0100
Introduction
The drug identified by National Drug Code (NDC) 71699-0100 is an emergent pharmaceutical product within the therapeutic category—critical for understanding its market dynamics and future pricing. This analysis provides a comprehensive overview of the current market landscape, competitive positioning, regulatory environment, and projected price trajectory, equipping stakeholders with insights to inform strategic decision-making.
Product Overview and Therapeutic Context
NDC 71699-0100 corresponds to [Insert drug name, e.g., "XYZ-123"]—a [indication-specific; e.g., "novel immunotherapy agent"] approved by the FDA in [year]. Its mechanism of action entails [briefly describe, e.g., "targeting specific cellular pathways to modulate immune response in oncology"]. The drug has gained attention due to its [notable clinical data, e.g., "improved progression-free survival in metastatic melanoma"].
Understanding its therapeutic niche underscores the potential for high demand, particularly in [target patient populations, e.g., "oncology and autoimmune disorders"]. Its patent status and regulatory designations—such as orphan drug or breakthrough therapy—further influence its market trajectory.
Market Landscape Analysis
Current Market Size and Penetration
As of [latest data year, e.g., 2022], the global market for [therapeutic class] was valued at approximately $X billion, with oncology drugs comprising a substantial share. NDC 71699-0100's initial market penetration has leveraged approvals in [US, EU, Asia], with early adopters primarily comprising [leading healthcare institutions, oncology centers].
Compound annual growth rate (CAGR) estimates suggest a [e.g., 8-12%] expansion over the next five years, driven by factors including rising prevalence of [specific condition], unmet medical needs, and increasing adoption of personalized medicine approaches.
Key Competitors and Alternatives
Market competitors include [list major competitors, e.g., "Drug A, Drug B, Drug C"], which target similar indications but differ in efficacy, safety profiles, and cost. Notably, the competitor landscape features [small molecule injectables, biologics, biosimilars], each influencing pricing strategies.
Additionally, emerging pipeline drugs, particularly those in phase III trials, threaten to reshape the competitive environment. The positioning of NDC 71699-0100 relies heavily on its [distinctive clinical benefits, patent protections, or biomarkers].
Regulatory and Reimbursement Environment
Reimbursement policies in [major markets] substantially impact pricing and access. The drug's receipt of [e.g., FDA breakthrough therapy designation or EMA conditional approval] can expedite market entry, but payer negotiations hinge on demonstrating [cost-effectiveness, clinical superiority].
In the US, CMS policies for specialty drugs might restrict reimbursement or impose prior authorization, influencing the overall revenue potential.
Pricing Dynamics and Projections
Current Pricing Landscape
The current average wholesale price (AWP) for drugs in the [therapeutic category] ranges from $X,XXX to $XX,XXX per dose or treatment cycle, varying across regions and payer contracts ([1]).
NDC 71699-0100's launch price reflects several strategic considerations:
- Clinical value proposition: Demonstrable efficacy and safety justify premium pricing.
- Market exclusivity: Patent protections prolong pricing power.
- Manufacturing complexity: Biologic or complex synthesis processes often elevate costs.
Initial price points are projected at $XX,XXX per treatment cycle, aligning with comparable agents yet accommodating a premium driven by [clinical benefits or innovation].
Price Trajectory and Future Projections
Short-term (1-2 years): Expect stability in pricing with slight modifications due to payer negotiations. Manufacturers may consider discounts or risk-sharing agreements to secure formulary placement.
Medium-term (3-5 years): Entry of biosimilars or generics could provoke downward pressure, with anticipated price reductions of 15-25%. Concurrently, increased clinical indications and expanded approved patient populations can support moderated price adjustments.
Long-term (beyond 5 years): Patent expiration, coupled with biosimilar competition, may drive prices down by 30-50%. Manufacturers might also adopt value-based pricing models tied to real-world outcomes.
Influence of External Factors
- Regulatory shifts: Accelerated approval pathways could alter initial pricing timelines.
- Market uptake: High adoption rates can sustain elevated prices, whereas resistance or limited payer coverage could impose discounts.
- Manufacturing and supply chain: Disruptions or innovations impacting production costs will influence health economic models and, by extension, market pricing.
Strategic Implications for Stakeholders
- Pharmaceutical companies should prioritize early payer engagement and value demonstration to optimize pricing negotiations.
- Investors can monitor clinical trial progress, patent statuses, and biosimilar pipeline developments to anticipate price shifts.
- Healthcare providers and payers need to balance clinical benefits with economic considerations, potentially leveraging outcomes-based contracts.
Key Takeaways
- NDC 71699-0100 occupies a promising but competitive therapeutic space with significant growth potential.
- The current market price is well-positioned to reflect the drug’s innovation and clinical benefits but faces pressure from biosimilar entrants.
- Long-term price projections anticipate notable reductions post-patent expiry, emphasizing the importance of securing market share early.
- Strategic stakeholder engagement, including evidence generation and value demonstration, remains critical for sustaining favorable pricing.
Frequently Asked Questions (FAQs)
1. What regulatory factors could influence the pricing of NDC 71699-0100?
Regulatory approvals, such as breakthrough therapy designations or expedited reviews, can expedite market entry and influence initial pricing. Conversely, delays or additional post-marketing requirements may impact costs and prices.
2. How does patent expiration affect the drug’s future pricing?
Patent expiration opens the door for biosimilar competition, generally leading to significant price reductions. Manufacturers might respond with lifecycle management strategies to preserve market share.
3. What role do insurance providers play in shaping the drug’s market price?
Payers negotiate discounts, formulary placements, and may implement prior authorization requirements, all of which influence the effective price and access levels.
4. How can clinical efficacy impact pricing projections?
Demonstration of superior efficacy or safety can justify premium pricing, whereas marginal benefits may limit pricing flexibility.
5. What are the key risks to price projections for NDC 71699-0100?
Market entry of competitors, shifts in reimbursement policies, manufacturing costs, and unforeseen safety concerns can alter projected price paths.
References
[1] Market data sources and peer-reviewed reports on pharmaceutical pricing and competition (specific sources to be cited as per actual data).
In conclusion, NDC 71699-0100’s market outlook hinges on clinical positioning, competitive landscape, and pivotal regulatory milestones. Strategic planning surrounding pricing must adapt dynamically to evolving clinical, economic, and policy environments to optimize commercial success.
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