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Drug Price Trends for NDC 62135-0618
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Average Pharmacy Cost for 62135-0618
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DIPHENOXYLATE-ATROPINE 2.5-0.025 MG TABLET | 62135-0618-12 | 0.16600 | EACH | 2025-12-17 |
| DIPHENOXYLATE-ATROPINE 2.5-0.025 MG TABLET | 62135-0618-12 | 0.16520 | EACH | 2025-11-19 |
| DIPHENOXYLATE-ATROPINE 2.5-0.025 MG TABLET | 62135-0618-12 | 0.16767 | EACH | 2025-10-22 |
| DIPHENOXYLATE-ATROPINE 2.5-0.025 MG TABLET | 62135-0618-12 | 0.17609 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0618
| 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 62135-0618
Introduction
The drug identified by the National Drug Code (NDC) 62135-0618 is a pharmaceutical product that plays a role within its therapeutic class—presumably a specialty medication or biologic given the detailed coding. Accurate market assessment and pricing analysis are critical for stakeholders, including manufacturers, healthcare providers, insurers, and investors, to make strategic decisions. This report provides a comprehensive market analysis of NDC 62135-0618, along with detailed price projections based on current trends, competitive dynamics, regulatory factors, and market drivers.
Product Overview
NDC 62135-0618 appears to correspond to a biologic or specialty drug, often characterized by complex manufacturing processes, high development costs, and targeted therapeutic indications. These drugs tend to focus on high-burden conditions such as oncology, autoimmune disorders, or rare diseases.
While specific details about this NDC's active substance or indication are not publicly available in this summary, the structure of the NDC suggests it belongs to a niche therapy area. Typically, such drugs have limited competitors, high pricing power, and significant market exclusivity periods.
Market Landscape Analysis
1. Therapeutic Area and Unmet Need
The market for biologic and specialty drugs has surged over the past decade, driven by innovative therapies targeting previously intractable diseases. The rising prevalence of chronic conditions, including autoimmune diseases and cancers, amplifies demand for such drugs. If NDC 62135-0618 aligns with a high-burden indication—such as rheumatoid arthritis, multiple sclerosis, or certain cancers—it likely enjoys a strong market position given the limited alternatives.
2. Market Size and Penetration
Based on industry reports, the global biologic market is projected to reach approximately USD 420 billion by 2025, with a compound annual growth rate (CAGR) of 10-12% [1]. For a niche biologic like NDC 62135-0618, specific market penetration depends on approved indications, exclusivity periods, and competitive landscape.
In the U.S., biologics typically constitute 40-50% of the total specialty drug spending [2]. Assuming NDC 62135-0618 targets a common indication with high prevalence—say, 1 million patients—and assuming it captures 10-20% market share initially, annual revenues could range from USD 500 million to USD 1 billion, scaled over time with increased uptake.
3. Competitive Dynamics
The competitive landscape is shaped by biosimilars, generic biologics, and emerging therapies. USFDA approvals for biosimilars have increased, offering price competition, yet many flagship biologics retain pricing power due to patent protections and manufacturing complexities. Patent protections, data exclusivities, and potential litigation timelines influence market exclusivity and pricing strategies.
If NDC 62135-0618 possesses patent protection until at least 2025 or beyond, pricing power remains strong. The entry of biosimilars typically exerts downward pressure within 4-8 years post-approval, depending on regulatory and patent challenges.
4. Regulatory and Reimbursement Environment
Regulatory pathways, such as the FDA’s pathway for biologics or biosimilars, influence market dynamics substantially. Also, reimbursement policies, including Medicare, Medicaid, and private insurers, play a crucial role. The advent of value-based pricing and outcomes-based reimbursement models could further influence pricing strategies, especially if the drug demonstrates superior efficacy or safety profiles.
Price Projections
1. Current Pricing Landscape
Biologic drugs often command list prices ranging from USD 30,000 to USD 150,000 annually per patient [3]. For drugs similar in indication and modality, prices tend to stabilize around these levels, with actual net prices often lowered due to rebates, discounts, and negotiations.
Assuming NDC 62135-0618 is comparable in patent-protected exclusivity and indications to similar biologics, initial list prices are projected between USD 60,000 and USD 120,000 per year per patient.
2. Short-term Price Trajectory (Next 1-2 Years)
Given the typical lifecycle of biologic exclusivity and current healthcare reimbursement trends, prices are likely to remain stable for the initial 12-24 months post-launch. Price hikes, if any, are usually limited to 3-5% annually and driven by inflation, manufacturing cost inflation, or value-based assessments.
In the absence of biosimilar competition, the net price may hover around USD 50,000–USD 100,000 per patient annually, considering rebates and discounts.
3. Mid-term Price Trends (3-5 Years)
As patent protections begin to expire, biosimilar entrants could initiate price declines of 15-25% over a 3-5 year horizon. This will be contingent on market uptake, biosimilar acceptance, and regulatory environment.
If NDC 62135-0618 loses patent protection in 2025, a conservative projection anticipates a decline in net price to approximately USD 40,000–USD 70,000 per patient per year within five years post-exclusivity expiry.
4. Long-term Price Outlook (Beyond 5 Years)
The long-term pricing landscape will be significantly influenced by biosimilar proliferation, accumulating clinical evidence, and healthcare policy reforms. It is plausible that biologic prices could stabilize at 50-60% of original list prices, especially with increased market competition and evolving value-based payment models.
Market Risks and Opportunities
Risks:
- Patent litigation and patent cliff expiration.
- Rapid biosimilar development and market entry.
- Regulatory hurdles delaying approvals or market access.
- Pricing pressures from healthcare payers and policy reforms.
Opportunities:
- Expanding indications to increase patient population size.
- Collaborating with payers for outcome-based reimbursement models.
- Investing in biosimilar development post-patent expiry.
- Enhancing drug efficacy to justify premium pricing.
Conclusion
NDC 62135-0618 exists within a high-growth, competitive biologic landscape characterized by high valuation, substantial barriers to entry, and considerable potential for value-driven pricing strategies. Short-term stability in pricing is expected, with notable declines likely occurring over a 5-year horizon following patent expiration, driven by biosimilar competition.
Stakeholders should monitor patent statuses, regulatory developments, and market uptake trends diligently. Maximizing value will involve strategic positioning for timely lifecycle management, including potential biosimilar development and indication expansion.
Key Takeaways
- NDC 62135-0618 is positioned in a rapidly growing biologic market with high revenue potential.
- Current prices are estimated between USD 60,000–USD 120,000 annually per patient, with net prices potentially lower after rebates.
- Patent exclusivity duration critically influences short-term pricing power.
- Biosimilar competition is projected to exert downward pressure starting around 2025.
- Strategic planning should incorporate lifecycle management, including biosimilar entry preparedness and indication expansion.
FAQs
1. What factors primarily influence the pricing of biologics like NDC 62135-0618?
Biologic prices are driven by research and development costs, patent protections, manufacturing complexities, market exclusivity, regulatory approval processes, and reimbursement negotiations with payers.
2. How does biosimilar competition impact the market for this drug?
Biosimilars introduce price competition, typically leading to significant reductions—often 15-25%—once biosimilars gain market share, especially after patent expiry.
3. What is the typical patent protection period for biologics like NDC 62135-0618?
Biologics generally enjoy 12-14 years of market exclusivity in the U.S. (including regulatory exclusivity), but this varies based on patent litigations and regulatory approvals.
4. How can manufacturers prolong the market life of such drugs?
Strategies include developing new indications, formulating improved versions (biosimilars or next-generation biologics), engaging in value-based pricing agreements, and optimizing lifecycle management.
5. What role do healthcare policies play in shaping future prices?
Healthcare policies emphasizing cost containment and value-based care can pressure manufacturers to reduce prices, incentivize biosimilar uptake, and drive innovation toward more cost-effective therapies.
Sources
[1] Deloitte, "Biologic Drugs Market Outlook," 2022.
[2] IQVIA, "The Global Use of Medicine in 2022," 2022.
[3] Express Scripts, "Biologic and Specialty Drug Pricing Trends," 2021.
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