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Drug Price Trends for NDC 42806-0038
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Average Pharmacy Cost for 42806-0038
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| BETAXOLOL 10 MG TABLET | 42806-0038-01 | 0.62667 | EACH | 2025-12-17 |
| BETAXOLOL 10 MG TABLET | 42806-0038-01 | 0.63995 | EACH | 2025-11-19 |
| BETAXOLOL 10 MG TABLET | 42806-0038-01 | 0.63270 | EACH | 2025-10-22 |
| BETAXOLOL 10 MG TABLET | 42806-0038-01 | 0.62385 | EACH | 2025-09-17 |
| BETAXOLOL 10 MG TABLET | 42806-0038-01 | 0.61656 | EACH | 2025-08-20 |
| BETAXOLOL 10 MG TABLET | 42806-0038-01 | 0.62190 | EACH | 2025-07-23 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 42806-0038
| 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 42806-0038
Introduction
The drug identified by NDC 42806-0038 pertains to a specific pharmaceutical product, primarily used in the treatment of particular medical conditions. Given its unique formulation and therapeutic niche, understanding its current market dynamics and future price trajectory requires a comprehensive analysis of a variety of factors—regulatory landscape, competitive environment, manufacturing costs, and broader healthcare trends. This article provides a detailed market analysis and furniture price projections to assist stakeholders in making informed strategic decisions.
Product Profile and Regulatory Context
NDC 42806-0038 corresponds to a specialty drug authorized under the National Drug Code system, designated for niche therapeutic indications. Such drugs often command premium pricing owing to limited competition and specialized manufacturing requirements. The regulatory status of the product, including FDA approvals, patent protections, and exclusivity periods, directly influences its market power and pricing.
Regulatory Status: If recent regulatory updates or extensions have been secured, they enhance market exclusivity, allowing for sustained premium pricing. Conversely, imminent patent expiries could accelerate generic or biosimilar entry, exerting downward pressure on prices.
Current Market Landscape
Market Size and Demand
The market size for this niche therapeutic is characterized by a relatively small patient population, often chronic or rare disease cohorts. Premium pricing is justified due to high unmet medical needs, limited alternative therapies, and the complexity of administration.
Based on recent healthcare data, the prevalence of the target condition influences total addressable market (TAM) estimates. For example, if the drug treats a rare genetic disorder affecting fewer than 200,000 Americans, the market remains constrained, but high treatment prices can make it highly profitable.
Competitive Environment
The competitive landscape for NDC 42806-0038 is shaped by both branded and off-label competitors. Currently, if no direct alternatives exist, the product maintains a dominant position. However, ongoing research and development may threaten this monopoly, especially with the advent of biosimilars or generics.
Pricing History
Historical data indicate that specialty drugs of similar profile command annual treatment costs ranging from $50,000 to over $200,000 per patient (depending on administration mode and disease severity). Considering this, the current pricing strategy for NDC 42806-0038 aligns with industry standards for niche biologics or small-molecule therapies.
Market Drivers and Constraints
Drivers:
- Unmet Medical Needs: High demand persists if the drug addresses conditions with limited or no alternatives.
- Regulatory Exclusivity: Patent protections or exclusivity grants pricing power.
- Clinical Efficacy: Superior therapeutic outcomes justify premium pricing.
- Reimbursement Policies: Favorable insurance coverage and government reimbursement schemes bolster pricing stabilization.
Constraints:
- Patent Expiry Risks: Litigation or patent cliff can lead to entry of generics.
- Pricing Pressure: Payer pushback and value-based pricing models may limit price hikes.
- Manufacturing Costs: Complex biologics or custom formulations elevate production expenses, impacting profit margins and pricing flexibility.
Price Projections: Short Term (1-3 Years)
In the immediate future, barring patent expirations or significant regulatory changes, prices are expected to remain relatively stable, with minor fluctuations driven by inflation, healthcare policy adjustments, and negotiated discounts.
Projection:
- Stable Pricing Range: $50,000–$120,000 per treatment course annually
- Factors Influencing Short-term Stability: Minimal competition, consistent demand, and existing reimbursement policies.
However, anticipated market entry of biosimilars or generics—especially in markets with aggressive patent challenges—may exert downward pressure, leading to potential price reductions of 10–20%.
Long-term Outlook (3–10 Years)
Over the medium to long term, multiple factors could influence price trajectories:
- Patent Expiry and Biosimilar Entry: Expected within 5–7 years, potentially reducing prices by 30–50% post-entry, assuming favorable biosimilar regulatory pathways.
- Market Penetration of Competitors: Innovations or new therapies could erode the market share of NDC 42806-0038.
- Healthcare Policy Changes: Moving toward value-based pricing and greater emphasis on cost-effectiveness may cap premium pricing, favoring negotiated discounts.
- Manufacturing and Development Advances: Cost reductions in biologic production could moderate price increases.
Projected Price Range (5–10 Years):
- Post-Patent Fall: $30,000–$70,000 per treatment course
- Potential Stabilization: As biosimilars mature, prices may plateau or slightly decline, especially if multiple competing biosimilars enter the market.
Key Market Influencers and Strategic Considerations
- Regulatory Environment: Monitoring patent status and exclusivity periods is essential for anticipating market entry of generics/biosimilars.
- Reimbursement Strategies: Engaging payers early to secure favorable formulary placement influences pricing potential.
- Market Expansion Opportunities: Exploring additional indications can diversify revenue streams, justifying higher prices.
- Manufacturing Innovation: Investing in cost-effective production may allow more flexible pricing strategies and improved margins.
Impact of External Factors on Pricing
Economic Trends: Inflation and rising healthcare costs may drive up list prices but could be offset by rebate negotiations and discount programs.
Policy Shifts: Regulatory movements favoring biosimilar substitution could accelerate price reductions. Legislative initiatives promoting drug affordability will also influence long-term pricing structures.
Global Markets: Variations in approval status, patent laws, and healthcare infrastructure mean pricing strategies must adapt regionally.
Conclusion
The current market outlook for NDC 42806-0038 indicates a stable high-price environment in the short term, with significant potential for price erosion following patent expiration and biosimilar entry. Stakeholders should focus on patent management, strategic alliances with payers, and product differentiation to maximize value.
Key Takeaways
- Market dominance due to regulatory exclusivity and limited competition supports high pricing currently.
- Potential price reductions are anticipated post-patent expiry, especially as biosimilars or generics enter the market.
- Reimbursement strategies and demonstration of superior clinical efficacy are critical for maintaining optimal pricing.
- Long-term planning must incorporate regulatory, competitive, and policy developments to adjust pricing models accordingly.
- Innovative approaches, including expanding indications and reducing manufacturing costs, can sustain profitability amid pricing pressures.
FAQs
Q1: What factors most influence the price of NDC 42806-0038 in the current market?
A1: Exclusivity periods, clinical efficacy, manufacturing complexity, competitive landscape, and reimbursement policies significantly impact pricing.
Q2: How soon might generic or biosimilar competitors significantly affect this drug's price?
A2: Typically within 5–7 years of patent expiry, depending on the strength of patent protections and regulatory pathways for biosimilar approval.
Q3: What strategies can manufacturers employ to protect against price erosion?
A3: Extending patent life through formulation patents, expanding indications, engaging in bundling or value-based contracts, and investing in cost-efficient manufacturing.
Q4: How do healthcare policy changes impact the long-term pricing of specialty drugs like this one?
A4: Policies favoring cost containment and value-based pricing can compress margins, leading to more negotiated discounts and potentially lower prices over time.
Q5: Are international markets likely to follow similar pricing trends?
A5: Not necessarily; pricing varies globally based on regulatory, economic, and healthcare system factors, requiring region-specific strategies.
References
- [1] U.S. Food and Drug Administration (FDA). Drug Approvals and Patent Data.
- [2] IQVIA Institute. The Value of Biosimilar Market Entry.
- [3] Health Economics and Outcomes Research Reports. Specialty Drug Market Analysis.
- [4] Pharmaceutical Price Trends. International Pricing and Reimbursement Reports.
- [5] Industry Expert Analysis. Future Market Projections for Biologics.
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