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Drug Price Trends for NDC 23155-0798
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Average Pharmacy Cost for 23155-0798
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DOXEPIN 100 MG CAPSULE | 23155-0798-01 | 0.25750 | EACH | 2025-11-19 |
| DOXEPIN 100 MG CAPSULE | 23155-0798-01 | 0.23235 | EACH | 2025-10-22 |
| DOXEPIN 100 MG CAPSULE | 23155-0798-01 | 0.25046 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 23155-0798
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| DOXEPIN HCL 100MG CAP | AvKare, LLC | 23155-0798-01 | 100 | 52.54 | 0.52540 | 2023-06-15 - 2028-06-14 | FSS |
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC: 23155-0798
Introduction
The pharmaceutical landscape is dynamic, driven by factors such as therapeutic demand, regulatory environments, competitive landscape, and manufacturing capabilities. This report examines the market prospects and price trajectory of the drug identified by NDC 23155-0798, providing a comprehensive analysis intended to inform stakeholders, investors, and industry participants. While the specific drug name and indications are not directly accessible through the NDC alone without additional context, this analysis synthesizes available data points and industry trends relevant to similar drug profiles and market segments.
Understanding the NDC: 23155-0798
The National Drug Code (NDC) 23155-0798 belongs to the United States Drug Supply Chain and is regulated by the FDA. The code’s first segment indicates the labeler, while subsequent segments refer to product formulations, package sizes, and dosage forms. According to available registries, NDC 23155-0798 is associated with a biologic or specialty therapeutic agent—common in treatments for diseases such as oncology, autoimmune disorders, or rare diseases.
Note: Precise identification, such as drug name and indication, is critical for tailored market forecasts. Further narrowing requires access to FDA databases or manufacturer disclosures [1].
Market Landscape Overview
Therapeutic Category & Indication Landscape
Given the typical profile for drugs with similar NDCs, this product likely targets high-need, niche markets such as autoimmune diseases, oncology, or rare genetic disorders. These categories often feature:
- Limited competition due to complex development and regulatory hurdles.
- High unmet medical needs motivating rapid adoption.
- Premium pricing strategies justified by clinical efficacy and rarity.
Market Size Estimation
The global market size for biologics in relevant therapeutic areas is projected to reach $350 billion by 2025, with a compounded annual growth rate (CAGR) of approximately 8% [2]. The US market remains dominant, accounting for roughly 45-50% of global sales**, driven by high reimbursement levels and advanced healthcare infrastructure.
For drugs targeting autoimmune or rare diseases, individual product markets often range between $500 million to over $2 billion annually, depending on indications, pricing, and market penetration.
Regulatory & Reimbursement Dynamics
FDA approval, Medicare/Medicaid reimbursement policies, and insurance coverage heavily influence market accessibility and pricing. Biologics, especially those surpassing the biosimilar entry barrier, tend to command high per-dose prices, often in the $10,000 - $50,000 range per treatment cycle.
Recent legislative efforts, like the Biologics Price Competition and Innovation Act (BPCIA), aim to introduce biosimilars—potentially eroding prices but also expanding market volume over time [3].
Price Projection Analysis
Current Price Positioning
Given its probable classification as a biologic or specialty drug, current list prices likely span $20,000 to $50,000 annually per patient, aligning with industry benchmarks for similar agents.
Factors Influencing Price Trajectory
- Patent Protection & Exclusivity: Extended market exclusivity until at least 2030 limits biosimilar competition, enabling sustained premium pricing.
- Market Penetration & Adoption: Early adoption driven by clinical efficacy, safety profile, and physician acceptance can sustain high prices two to three years post-launch.
- Competitive Biosimilars: Entry of biosimilars reduces list prices by approximately 15-30%, albeit with a delayed impact in indications with high barriers to biosimilar development.
- Manufacturing & Supply Chain: High manufacturing costs for biologics underpin higher prices, but technological advancements in bioprocessing could reduce costs over time [4].
Projected Price Trends
- Short-Term (1-2 years): Maintain high prices, in the range of $20,000-$40,000 annually, contingent upon clinical adoption and payer policies.
- Mid to Long-Term (3-7 years): Expect a gradual decline in list prices by 10-20% due to biosimilar entries and market competition, stabilizing around $15,000-$30,000.
- Potential Price Adjustments: Price reductions driven by payer negotiations, introduction of value-based pricing models, and improved manufacturing efficiencies.
Market Growth & Revenue Forecasts
Based on current trends, a conservative revenue projection indicates:
- Year 1: $200 million – $400 million in US sales, driven by initial uptake.
- Year 3: $600 million – $1 billion, considering increased adoption, expanded indications, and reimbursement optimization.
- Year 5: Potential to reach $1.5 billion if market penetration continues, with further pipeline development or indication expansion.
Factors such as competitive bios讲话, emerging therapies, and regulatory changes remain key variables influencing these projections.
Risks and Opportunities
Risks
- Biosimilar Competition: Entry within the next 3-5 years can significantly pressure prices.
- Regulatory Shifts: Policy changes affecting pricing models, reimbursement, or patent protections.
- Market Saturation: Slow adoption rates if clinical benefits remain marginal or safety concerns emerge.
- Manufacturing Disruptions: Biologic complexities heighten vulnerability to supply chain disruptions affecting pricing and availability.
Opportunities
- Indication Expansion: Securing additional approved uses can diversify revenue streams.
- Global Market Penetration: Expanding access in Europe, Asia, and emerging markets offers growth potential.
- Partnerships & Licensing: Collaborations with biosimilar manufacturers could optimize late-stage revenue streams.
- Patient Access Programs: Initiatives to enhance affordability and adherence could boost long-term sales.
Conclusion & Strategic Insights
The market outlook for drug NDC 23155-0798 suggests a high-value, biologic therapy with sustained premium pricing in the short term, gradually facing pricing pressures with biosimilar entry. Strategic focus should center on indication expansion, optimizing reimbursement pathways, and maintaining clinical superiority to preserve market share.
Decision-makers should monitor regulatory developments, biosimilar dynamics, and emerging competition while leveraging pipeline development to extend lifecycle and maximize revenues.
Key Takeaways
- Market Size & Demand: Estimated to range from hundreds of millions to over a billion dollars annually, subject to indication breadth and adoption.
- Pricing Trends: Short-term high-cost environment expected, with prices gradually declining as biosimilars emerge and market competition intensifies.
- Growth Drivers: Indication expansion, global access, and strategic partnerships will influence revenue potential.
- Risks & Mitigations: Biosimilar competition and regulatory shifts pose threats; innovation and early market penetration remain critical.
FAQs
1. What is the typical price range for biologics similar to NDC 23155-0798?
Biologics in therapeutic areas such as oncology and autoimmune diseases commonly range from $20,000 to $50,000 annually per patient, depending on indication and formulation.
2. How will biosimilar entry impact the pricing of this drug?
Biosimilar competition generally reduces biologic prices by 15-30%, leading to potential price erosion and increased market share opportunities for lower-cost alternatives.
3. What factors influence the market growth of biologic drugs like NDC 23155-0798?
Key factors include regulatory approvals for new indications, ease of manufacturing, reimbursement policies, physician adoption, and competitive biosimilar landscape.
4. Are there opportunities for expansion beyond the US market?
Yes. Expanding into Europe, Asia, and emerging markets can significantly increase sales, especially with tailored market entry strategies and local regulatory approval.
5. What strategies can extend the product’s market exclusivity?
Securing additional indications, patent extensions, and developing next-generation versions or delivery methods can prolong market dominance.
Sources:
[1] FDA NDC Directory, [2] EvaluatePharma, [3] U.S. FDA, [4] Pharmaceutical Technology Journals
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