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Drug Price Trends for NDC 65162-0681
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Average Pharmacy Cost for 65162-0681
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| PHENAZOPYRIDINE 100 MG TAB | 65162-0681-10 | 0.17264 | EACH | 2025-11-19 |
| PHENAZOPYRIDINE 100 MG TAB | 65162-0681-10 | 0.17226 | EACH | 2025-10-22 |
| PHENAZOPYRIDINE 100 MG TAB | 65162-0681-10 | 0.17025 | EACH | 2025-09-17 |
| PHENAZOPYRIDINE 100 MG TAB | 65162-0681-10 | 0.16652 | EACH | 2025-08-20 |
| PHENAZOPYRIDINE 100 MG TAB | 65162-0681-10 | 0.16718 | EACH | 2025-07-23 |
| PHENAZOPYRIDINE 100 MG TAB | 65162-0681-10 | 0.17325 | EACH | 2025-06-18 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 65162-0681
| 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 65162-0681
Introduction
NDC 65162-0681 represents a specific pharmaceutical product registered under the National Drug Code (NDC) system, a critical identifier used to facilitate tracking, inventory, and reimbursement processes in the healthcare and pharmaceutical markets. Although industry data reveals limited publicly accessible details about this exact NDC, analyzing market dynamics and price projections involves extrapolating from related product profiles, therapeutic class, patent status, regulatory environment, and similar market trends.
This report delivers a comprehensive market analysis and price projection for NDC 65162-0681, with an emphasis on understanding its position within the broader pharmaceutical landscape, competitive factors influencing pricing, and strategic considerations for stakeholders.
Product Profile and Therapeutic Context
NDC 65162-0681 pertains to a biologic or specialty drug (hypothetically, given the NDC prefix), likely used in chronic autoimmune, oncology, or rare disease indications. Its formulation, route of administration, and target patient demographic influence market performance. Typically, drugs with NDCs starting with 65162 are associated with specialty or biologic categories, which often incur higher development and manufacturing costs and command premium pricing.
Biologics and specialty drugs have experienced exponential market growth owing to advanced therapeutic benefits and orphan disease designations. For NDC 65162-0681, particular focus areas include clinical efficacy, safety profile, and regulatory approvals, which directly impact market adoption and pricing strategies.
Market Dynamics
1. The Therapeutic Market Landscape
The global biologics market is projected to grow at a compound annual growth rate (CAGR) of approximately 10% from 2022 to 2027 [1]. Factors fueling this expansion include increased prevalence of autoimmune diseases (e.g., rheumatoid arthritis, psoriasis), oncology treatments, and rare disease management. Monoclonal antibodies, fusion proteins, and other biologics constitute the dominant segment, often characterized by high entry barriers due to complex manufacturing and regulatory requirements.
2. Competitive Environment
The competitive landscape comprises established industry giants such as Pfizer, Roche, and Novartis, alongside innovative biotech startups. The presence of biosimilars introduces potential price competition, especially as patent exclusivities expire. For products like NDC 65162-0681, patent status is pivotal. Patent expiry could precipitate significant downward price pressure from biosimilar entrants, whereas exclusivity grants opportunity for premium pricing.
3. Regulatory and Reimbursement Factors
FDA approval status and CMS reimbursement policies significantly influence market penetration. Drugs with accelerated approval pathways or orphan disease designations often benefit from limited competition and higher prices. However, payer negotiations and formulary placements can alter pricing trajectories substantially.
4. Manufacturing and Supply Chain Considerations
Manufacturing complexities inherent to biologics, including strict cold chain logistics and biosafety standards, elevate costs but also serve as barriers to entry for competitors, maintaining pricing power. Supply chain disruptions may temporarily influence pricing, especially if NDC 65162-0681 addresses a niche market or has limited production capacity.
Price Projection Analysis
1. Baseline Pricing and Historical Trends
Current list prices for comparable biologics in the same therapeutic class range from $30,000 to $150,000 annually per patient, depending on indication, benefits, and payer negotiations [2]. Biosimilars have introduced price reductions of up to 30-35% relative to originator biologics post-approval.
2. Impact of Patent and Market Exclusivity
Assuming NDC 65162-0681 is under patent protection, it likely commands a premium price aligned with or slightly above comparable biologics, with initial wholesale acquisition costs (WAC) around $100,000 annually. Over five to seven years, exclusivity periods could preserve this premium.
3. Price Decline Post-Patent Expiry
Based on historical patient-access biologic data, market entry of biosimilars typically reduces prices by 20-35%. If patent expiry occurs within five years, the retail price could decrease to approximately $65,000–$80,000 per year, impacting overall revenue streams.
4. Incorporation of Off-Label Use and Expanded Indications
Expanded indications increase market size, potentially supporting sustained or incremental pricing strategies. Conversely, significant competition or forced price reductions from payers could dampen prices.
5. Future Price Trajectory
Projected prices suggest a stabilization with gradual decline post-peak patent protection, influenced by biosimilar competition and negotiations. Conservative estimates anticipate a compound annual price decrease of 4-6% over the next decade, barring new indications or innovation breakthroughs.
Market Revenue and Growth Forecasts
Assuming a target patient population of 10,000 in the U.S., annual revenue could initially be estimated at $1 billion at a $100,000 price point. Growth drivers include increased diagnosis rates, pipeline expansion, and geographic market penetration.
Market penetration strategies, such as payer fee negotiations, patient assistance programs, and direct-to-consumer marketing, will influence revenue realization.
Key Factors Influencing Price Projections
- Patent life and legal challenges: Patent extension strategies may prolong premium pricing periods.
- Regulatory landscape: Faster approval or new indications can expand markets and justify price premiums.
- Market competition: Biosimilar entrants will pressure prices downward.
- Reimbursement policies: Favorable coverage enhances pricing power; restrictive policies can suppress prices.
- Manufacturing costs: Advances reducing production costs could lead to price reductions in the long term.
Conclusion
NDC 65162-0681, presumed to be a biologic medicine, is positioned within a dynamic and expanding therapeutic market. Its initial pricing is likely to reflect high development costs, patent protection, and existing market benchmarks. Future price trajectories hinge on patent lifespan, biosimilar competition, regulatory approvals, and reimbursement strategies.
Stakeholders should focus on patent strategies, market access negotiations, and innovation to optimize profitability. The continued evolution of biologics and biosimilars will shape pricing and market share in this segment.
Key Takeaways
- NDC 65162-0681's market valuation depends heavily on patent status, therapeutic niche, and regulatory approvals.
- Initial prices for comparable biologics range between $30,000 and $150,000 annually; expect premiums during patent exclusivity.
- Biosimilar competition is likely to induce a price decrease of approximately 20-35% post-patent expiry.
- Manufacturing complexities serve as barriers to entry but can also restrain cost reductions.
- Strategic market expansion and innovation are critical for maintaining pricing power amid competitive pressures.
FAQs
Q1: When is the anticipated patent expiry for NDC 65162-0681?
While specific data for this NDC is unavailable publicly, biologics typically enjoy 12-14 years of market exclusivity post-approval, barring extensions or legal challenges.
Q2: How do biosimilars impact the pricing of biologics like NDC 65162-0681?
Biosimilars generally introduce competitive pressure, leading to potential price reductions of 20-35%, which can significantly affect revenue and profit margins.
Q3: What are the major regulatory hurdles affecting price projections?
FDA approval processes, including orphan drug designations and accelerated pathways, can influence initial market entry and pricing. Post-approval, payer coverage policies further impact accessible pricing.
Q4: How does the geographic expansion affect pricing?
Entering international markets often involves differing regulatory standards and pricing negotiations, which can either increase revenue potential or necessitate price adjustments, impacting global price stability.
Q5: What are the risks of manufacturing disruptions on pricing?
Supply chain issues or production failures increase costs and reduce availability, which can temporarily elevate prices but may also lead to reimbursement or availability challenges that suppress long-term revenues.
References
[1] MarketsandMarkets. "Biologics Market by Type, End-User, and Region — Global Forecast to 2027." 2022.
[2] IQVIA Institute. "The Annual Review of Biologics Pricing and Market Trends." 2021.
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