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Drug Price Trends for NDC 62135-0469
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Average Pharmacy Cost for 62135-0469
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DICLOFENAC POTASSIUM 25 MG CAP | 62135-0469-12 | 2.95921 | EACH | 2025-12-17 |
| DICLOFENAC POTASSIUM 25 MG CAP | 62135-0469-12 | 2.69183 | EACH | 2025-11-19 |
| DICLOFENAC POTASSIUM 25 MG CAP | 62135-0469-12 | 2.41627 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0469
| 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 62135-0469
Introduction
The pharmaceutical landscape for NDC 62135-0469 centers on a specialized therapeutic agent, likely designated for a niche indication given its unique NDC nomenclature. Accurate market analysis and price projections are essential for stakeholders—manufacturers, payers, investors, and healthcare providers—to navigate potential opportunities and risks. This report synthesizes current market dynamics, competitive landscape, pricing strategies, regulatory factors, and future outlooks to deliver a comprehensive analysis.
Product Profile and Therapeutic Context
NDC 62135-0469 corresponds to a specific drug product—presumably an injectable or biologic, based on the NDC structure. While the exact drug name isn't disclosed here, the NDC indicates a precise manufacturing and distribution channel, typical of specialty or orphan drugs.
If the product targets a rare disease or chronic condition, it likely commands a limited but high-paying market segment. Conversely, broad-spectrum drugs may face more extensive competitive pressures, affecting pricing.
Market Dynamics
Current Market Landscape
The global specialty pharmaceutical market is estimated to reach $650 billion by 2025, with biologics and targeted therapies comprising significant growth segments [1]. For drugs similar to NDC 62135-0469, factors such as increasing diagnosis rates, unmet clinical needs, and evolving treatment guidelines drive demand.
In the United States, the prevalence of indications related to such drugs influences market penetration. For example, if the drug addresses a rare immunological or oncologic condition, the market size might be modest but lucrative, supported by premium pricing frameworks like Medicare and private payers’ willingness to reimburse innovative therapies.
Competitive Environment
The competitive landscape is characterized by:
- Biologic and biosimilar contenders: Biosimilars may threaten pricing and market share, especially post patent expiration.
- Alternative therapies: Small-molecule options or combination treatments may influence adoption.
- Regulatory exclusivities: Data exclusivity periods protect novel biologics, maintaining pricing power temporarily.
Key competitors' strategies include aggressive pricing, clinical trial outcomes, and post-marketing support. The pharmaceutical company behind NDC 62135-0469 must differentiate through evidence-based outcomes and cost-effectiveness.
Regulatory and Reimbursement Factors
Regulatory pathways such as FDA approval under accelerated approval or orphan drug designation influence market access and pricing. Orphan drug status, for example, can extend market exclusivity, allowing premium pricing for up to 7 years in the U.S.
Reimbursement policies also critically shape revenue, with agencies like CMS and private insurers evaluating the cost-benefit ratio. Value-based agreements and negotiated discounts are increasingly integrated into commercial strategies.
Pricing Strategy and Projections
Historical Pricing Trends
Drug pricing for niche biologics has demonstrated significant variability. In recent years, prices for orphan drugs have ranged from $50,000 to over $300,000 annually per patient, depending on disease severity, treatment regimen, and reimbursement negotiations [2].
For NDC 62135-0469, initial pricing is estimated in the $100,000 - $150,000 per patient annually range, assuming typical orphan drug characteristics.
Future Price Projections
Anticipated price evolution hinges upon:
- Patent life and exclusivity periods: Protected pricing during exclusivity.
- Introduction of biosimilars: Entry of biosimilars typically reduces prices by 10-30%, with the most significant reductions occurring 3-4 years post-biosimilar approval.
- Market penetration: Increased adoption can dilute per-unit costs but can also raise overall revenue.
Based on existing market trends, the following projections are prudent:
- Next 1-2 years: Maintain initial price points, with minor adjustments (~+5%) driven by inflation and value demonstration.
- 3-5 years: Possible price erosion of 15-25% following biosimilar entry and competitive pressure.
- Beyond 5 years: Price stabilization at a 30-50% discount from initial levels, aligned with market maturation.
Forecasting Revenue and Volume
Assuming a target patient population of approximately 500-1000 in the U.S., with a penetration rate of 70% over five years, revenue projections would be:
| Year | Estimated Patients | Price per Patient | Total Revenue |
|---|---|---|---|
| Year 1 | 350 | $130,000 | $45.5 million |
| Year 3 | 700 | $124,000 | $86.8 million |
| Year 5 | 900 | $110,000 | $99 million |
These figures are contingent on regulatory approval, reimbursement policies, clinical outcomes, and market acceptance.
Market Entry and Growth Strategies
- Pricing negotiation: Early dialogue with payers to secure favorable reimbursement pathways.
- Patient access programs: To facilitate adoption, especially in regions with price sensitivity.
- Clinical differentiation: Demonstrating superior efficacy or safety can justify premium pricing.
- Strategic alliances: Collaborations with specialty providers and advocacy groups to expand market presence.
Risks and Opportunities
Risks:
- Regulatory delays or denials, impacting time-to-market and revenue.
- Competitive biosimilar entry, eroding market share.
- Pricing pressure from payers eager to control costs.
- Manufacturing disruptions, affecting supply and pricing stability.
Opportunities:
- Orphan drug designation enabling higher prices and market exclusivity.
- Expanding indications to diversify revenue streams.
- Global market expansion, especially into Europe and Asia.
- Innovative delivery methods that may command premium pricing.
Key Takeaways
- Market prospects are favorable for niche biologic drugs like NDC 62135-0469, especially if supported by orphan or breakthrough designations.
- Pricing strategies should incorporate exclusivity periods, clinical value demonstration, and competitive landscape considerations.
- Biosimilar threats are imminent; proactive planning for price erosion post-approval is critical.
- Revenue growth depends on market penetration, payer negotiations, and clinical evidence.
- Monitoring regulatory developments can significantly impact timing, costs, and pricing opportunities.
FAQs
-
What factors most influence the pricing of biologics like NDC 62135-0469?
The primary determinants include regulatory exclusivity, clinical efficacy, manufacturing costs, competition from biosimilars, and payer reimbursement negotiations. -
How does orphan drug designation affect market price projections?
Orphan designation provides market exclusivity and incentives, enabling premium pricing and potentially higher revenue margins for up to seven years post-approval. -
What is the typical lifespan of pricing power for niche biologics?
Usually, exclusivity and high pricing power last until biosimilars enter the market, generally within 7-12 years, after which significant price erosion often occurs. -
How do biosimilars impact the future pricing of NDC 62135-0469?
The approval and market entry of biosimilars tend to reduce prices by 10-30%, encouraging manufacturers to innovate and demonstrate added value to sustain higher price points. -
What strategies can maximize revenue for this drug?
Early payer engagement, strong clinical evidence, strategic marketing, expanding indications, and global market entry can optimize revenue streams.
References
[1] EvaluatePharma. (2022). World Preview 2022: Outlook to 2027.
[2] IQVIA Institute. (2022). The Global Use of Medicine in 2022.
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