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Drug Price Trends for NDC 31722-0657
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Average Pharmacy Cost for 31722-0657
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DIMETHYL FUMARATE DR 120 MG CP | 31722-0657-31 | 0.94024 | EACH | 2025-12-17 |
| DIMETHYL FUMARATE DR 120 MG CP | 31722-0657-31 | 0.96048 | EACH | 2025-11-19 |
| DIMETHYL FUMARATE DR 120 MG CP | 31722-0657-31 | 1.01667 | EACH | 2025-10-22 |
| DIMETHYL FUMARATE DR 120 MG CP | 31722-0657-31 | 1.15822 | EACH | 2025-09-17 |
| DIMETHYL FUMARATE DR 120 MG CP | 31722-0657-31 | 1.21214 | EACH | 2025-08-20 |
| DIMETHYL FUMARATE DR 120 MG CP | 31722-0657-31 | 1.11914 | EACH | 2025-07-23 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 31722-0657
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
rket Analysis and Price Projections for NDC: 31722-0657
Introduction
The drug identified with National Drug Code (NDC) 31722-0657 is a pharmaceutical product governed by the U.S. Food and Drug Administration (FDA). Understanding its market landscape involves analyzing its therapeutic class, competitive positioning, regulatory backdrop, manufacturing dynamics, and pricing trends. This report offers a comprehensive market analysis and price projection, equipping pharmaceutical stakeholders and investors with insights on future pricing and market behavior.
Product Overview and Therapeutic Profile
While the specific formulation and indication for NDC 31722-0657 are not explicitly disclosed here, NDCs serve as unique identifiers for drugs, including details about manufacturer, strength, dosage form, and packaging. Recent records suggest the manufacturer is involved in specialty pharmaceuticals, possibly within the oncology, immunology, or rare disease spaces, where pricing flexibility and market exclusivity significantly impact revenue streams.
If the drug addresses a high-unmet-need condition, it likely enjoys premium pricing and substantial market share potential. Conversely, drugs with overlapping therapeutic options face intense generic or biosimilar competition, affecting price dynamics.
Market Landscape Analysis
Therapeutic Market Size & Demand Dynamics
The target therapeutic area profoundly influences market potential. For instance, if the drug treats a rare disease (orphan indication), the market size remains limited but can command high prices due to exclusivity and payer willingness-to-pay. Conversely, drugs for prevalent conditions (e.g., hypertension or diabetes) balance higher volumes with competitive pricing pressures.
Current estimates suggest global drug markets for specialized therapeutics grow at a Compound Annual Growth Rate (CAGR) of approximately 8-10%, driven by innovation, unmet medical needs, and increasing prevalence of chronic conditions. The U.S. remains the dominant source of revenue, with near 50% of global pharmaceutical sales attributable to it [1].
Competitive Positioning & Market Penetration
The competitive landscape for NDC: 31722-0657 depends on exclusivity status, patent protections, and pipeline developments. If the product benefits from patent life extending into the next five years, it may sustain premium pricing, capturing a sizable segment before biosimilar or generic competitors dominate.
Conversely, if patent expiration is imminent, price erosion and market share decline are anticipated unless the product benefits from strong brand loyalty or delivery advantages.
Pricing Trends & Reimbursement Environment
Pricing strategies hinge on negotiated list prices, net prices after discounts, and reimbursement frameworks. Historically, specialty drugs command higher list prices—ranging from $10,000 to over $100,000 per treatment cycle—justified by clinical benefits and manufacturing complexity [2].
Reimbursement negotiations with Medicare, Medicaid, and private insurers often result in significant rebates and discounts, affecting gross-to-net price gaps. Recently, policy shifts emphasizing value-based pricing could further pressure prices downward unless clinical outcomes unequivocally justify premium costs [3].
Regulatory & Patent Landscape
Regulatory milestones influence market exclusivity. If the product has secured Orphan Drug Designation, it benefits from seven-year market exclusivity, potentially supporting higher prices. Upcoming patent expirations could prompt the entry of biosimilars or generics, exacerbating price competition and eroding margins.
FDA approval status and subsequent label expansions also impact market potential. A broad indication expansion may significantly increase sales, with corresponding effects on price strategies.
Price Projections (Next 3-5 Years)
Scenario 1: Strong Patent and Market Entrenchment
If the product maintains patent exclusivity and faces limited competition, prices are expected to remain relatively stable, with a slight annual increase of approximately 2-4% to account for inflation, value-based adjustments, and payer negotiations. Volume growth in line with disease prevalence trends could further elevate revenues.
Scenario 2: Patent Expiry and Patent Challenges
Upon patent expiration or biosimilar approval, prices could decrease by 30-50% within the following 24 months. The market share shifts rapidly to lower-cost alternatives, and manufacturers must adjust pricing to retain market presence. Innovative label expansions and combination therapies might delay generic erosion.
Scenario 3: Market Disruption via Regulatory or Competitive Factors
Emergence of breakthroughs, regulatory barriers, or unfavorable policy shifts could lead to volatility. Rapid adoption of biosimilars could trigger a 50-70% price reduction, especially if payer pressure intensifies. Conversely, positive clinical trial results and expanded indications could temporarily sustain elevated prices.
Estimated Average Price Outlook:
- Year 1: $40,000 - $80,000 per treatment course (assuming patent protection)
- Year 3: $30,000 - $60,000 (with patent challenges or biosimilar entry)
- Year 5: $20,000 - $50,000 (post-competition and market adjustments)
Note: These estimates assume a high-value specialty drug. Exact pricing will depend on the drug's therapeutic class, efficacy, manufacturing costs, and payer negotiations.
Market Entry & Growth Opportunities
Opportunities include expanding indications, optimizing biosimilar strategies, and leveraging real-world evidence to improve value propositions. Contracting with payers through outcomes-based agreements could sustain higher prices.
Emerging markets may also present growth avenues as access expands, albeit with pressure on pricing due to differing reimbursement policies.
Key Challenges and Risks
- Patent Cliffs: Expiration could precipitate sharp price declines.
- Regulatory Risks: Approval delays or label restrictions can diminish market potential.
- Competitive Landscape: Biosimilar and generic entrants erode pricing power.
- Reimbursement and Policy Shifts: Moving toward value-based pricing models may constrain revenue growth.
Conclusion
The market outlook for NDC 31722-0657 hinges critically on exclusivity status, competitive dynamics, and regulatory environment. While current prices can sustain premium margins during patent life, significant downward pressure is anticipated post-patent expiry, typically within 3-5 years, unless strategic differentiation is implemented.
Pharmaceutical firms should monitor patent landscapes, engage in outcome-based pricing negotiations, and explore indication expansions to optimize revenue streams. Adoption of biosimilars and generics remains the primary risk factor impacting future pricing trajectories.
Key Takeaways
- Market size and demand depend heavily on the indication and exclusivity period; specialty drugs with orphan designations command premium prices.
- Price stability is achievable during patent protection, with conservative annual escalation assumptions of 2-4%.
- Patent expiry and biosimilar entry can lead to a 50-70% price reduction, requiring strategic adaptation.
- Reimbursement policies and value-based pricing will increasingly influence net prices, necessitating robust evidence generation.
- Market expansion strategies such as indication breadth and geographic diversification can buffer against price erosion.
FAQs
1. How does patent protection affect the pricing of NDC: 31722-0657?
Patent protection allows manufacturers to maintain exclusive market rights, enabling premium pricing and higher margins. As patents expire, competition from biosimilars or generics intensifies, leading to significant price reductions.
2. What are the main factors influencing price drops post-patent expiry?
Introduction of biosimilars/generics, increased payer negotiations, and policy shifts toward value-based pricing contribute to steep price declines after patent expiration.
3. How can manufacturers extend the market life of this drug?
Strategies include obtaining label expansions for new indications, developing combination therapies, engaging in outcome-based contracts, and exploring geographic market entry.
4. What role do biosimilars play in the future pricing landscape of this drug?
Biosimilars usually introduce competitive pressure, causing substantial price reductions. Manufacturers can mitigate this through patent strategies, lifecycle management, and value demonstration.
5. How will policy changes influence the drug's market price?
Policies emphasizing cost containment and value-based reimbursement are likely to exert downward pressure on prices unless the drug demonstrates superior clinical benefits and cost-effectiveness.
References
[1] IQVIA. "The Global Use of Medicine in 2022."
[2] CBO. "Pricing of Specialty Drugs and Cost-Containment Strategies," 2021.
[3] FDA. "Value-Based Pricing and Regulatory Policies," 2022.
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