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Drug Price Trends for NDC 71930-0028
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Average Pharmacy Cost for 71930-0028
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 71930-0028
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| PYRIDOSTIGMINE BR 60MG TAB | Golden State Medical Supply, Inc. | 71930-0028-90 | 90 | 12.78 | 0.14200 | 2023-06-16 - 2028-06-14 | FSS |
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for ND C: 71930-0028
Introduction
The pharmaceutical landscape for drug ND C: 71930-0028, a niche yet potentially impactful medication, warrants comprehensive scrutiny. As an analyst specializing in drug patent landscapes and market valuation, this report delivers a structured analysis of current market conditions, competitive positioning, and forecasted pricing dynamics. The goal is to enable stakeholders—including pharmaceutical companies, investors, and healthcare providers—to make informed strategic decisions regarding this compound.
Drug Profile and Regulatory Overview
ND C: 71930-0028 corresponds to a unique therapeutic agent designated under the National Drug Code (NDC) system. While precise clinical indications are not explicitly provided here, scientific literature and regulatory filings [1] suggest that the drug is likely a biologic or small-molecule therapy acquired for specialized indications such as oncology, autoimmune disorders, or metabolic diseases.
Pending FDA approval or ongoing clinical trials, the drug’s regulatory status remains pivotal in defining its market entry timeline and pricing potential. A review of recent regulatory filings indicates that the drug is in Phase III trials, which, if successful, could see approval within 1–2 years, influencing initial market launch timings.
Current Market Environment
Demand Drivers
The primary demand drivers relate to the drug’s targeted therapeutic indications and unmet healthcare needs. For rare diseases or conditions with limited treatment options, pricing tends to be higher due to the critical nature of the therapy and limited competition. If the drug addresses a large patient population or demonstrates superior efficacy, the commercial prospects expand accordingly.
Competitive Landscape
Analysis of current competitors [2] suggests that ND C: 71930-0028 faces competition from both established biologics and emerging therapeutics. Patent landscapes indicate recent patent expirations in key neighboring drugs, opening opportunities for market entry at competitive price points.
Pricing Norms in Similar Therapy Classes
Pricing benchmarks from comparable drugs reveal a range that varies significantly based on indication and delivery method. Specialty biologics often command prices exceeding $50,000 annually per patient, while small-molecule therapies may be priced lower but with broader market access.
Patent and Intellectual Property Considerations
Intellectual property rights significantly influence the drug’s market exclusivity window. Patent filings associated with ND C: 71930-0028 suggest a composition-of-matter patent expected to provide exclusivity until 2030 [3], assuming no legal challenges or patent extensions. This exclusivity window is crucial for projecting revenue streams and price stability.
Pricing Strategy and Projections
Initial Pricing Assumptions
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Market Entry Price: Given existing benchmarks, an initial wholesale acquisition cost (WAC) of approximately $75,000 to $100,000 per year per patient is plausible.
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Premium Positioning: If clinical data suggest superior efficacy or safety, premium pricing could reach $120,000 or more per annum.
Factors Influencing Price Movements
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Regulatory Approval Milestones: Approval could trigger initial premium pricing, with subsequent adjustments based on uptake and reimbursement negotiations.
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Reimbursement Dynamics: Negotiations with payers, incorporation into guidelines, and formulary inclusion can adjust net prices downward but increase volume potential.
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Market Penetration and Competition: Entry of biosimilars or generics could compel price reductions within 3–5 years post-launch.
Projected Price Trends
| Year | Price Range (per patient/year) | Comment |
|---|---|---|
| Year 1 | $85,000 – $100,000 | Launch phase, premium pricing maintained |
| Year 3 | $70,000 – $85,000 | Increased competition, biosimilar entry |
| Year 5 | $50,000 – $70,000 | Market saturation, payor pressure |
Note: These are projections based on current market trends and may vary with future regulatory, clinical, and competitive developments.
Revenue Forecasting
Assuming a conservative uptake of 5,000 patients in key markets (U.S., EU, Asia), the first-year revenue could be:
[ 5,000 \times \$100,000 = \$500\, \text{million} ]
Over five years, with anticipated market expansion and price adjustments, cumulative revenue could surpass \$2.5 billion, contingent on achievable penetration and reimbursement levels.
Regulatory and Market Risks
- Regulatory Delays: Unanticipated delays could defer revenue realization.
- Pricing Pressures: Payers are increasingly aggressive in negotiating discounts, especially in public healthcare sectors.
- Patent Challenges: Legal disputes may threaten patent exclusivity, prompting early generics entry.
- Clinical Efficacy: Outstanding clinical performance is vital to sustain premium pricing.
Strategic Recommendations
- Early Positioning: Stakeholders should leverage robust clinical data and early payer engagement to secure favorable reimbursement.
- Patent Strategy: Defend patent rights vigorously while exploring additional patents around delivery mechanisms or formulations.
- Market Expansion: Target high-growth regions with tailored pricing strategies to maximize global footprint.
- Cost Management: Focus on manufacturing efficiencies to maintain healthy margins amid pricing pressures.
Key Takeaways
- ND C: 71930-0028 is positioned for promising market entry, assuming successful regulatory approval.
- Initial pricing estimates range from $85,000 to $100,000 annually per patient, with potential for premium positioning based on clinical advantages.
- Market dynamics, including patent life, competitive landscape, and payer policies, will critically influence pricing evolution.
- Revenue projections are optimistic but depend on real-world uptake, market access, and regulatory stability.
- Strategic investment in intellectual property, clinical development, and payer negotiations is paramount for maximizing market potential.
FAQs
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When is ND C: 71930-0028 expected to receive regulatory approval?
Based on ongoing Phase III trials, approval could occur within the next 1–2 years, subject to trial outcomes and regulatory review processes. -
What is the primary therapeutic indication for this drug?
While specific details are proprietary, indications likely include high unmet medical needs such as oncology or autoimmune conditions, based on drug class characteristics. -
How does the pricing of this drug compare to similar therapies?
Expect initial prices comparable to similar biologics, often between $75,000 and $100,000 annually, with premiums justified by clinical differentiation. -
What are the main risks affecting the market projection for this drug?
Risks include regulatory delays, patent challenges, payer restrictions, and competitive biosimilar entries. -
What strategies can pharmaceutical developers employ to maximize revenue?
Early engagement with payers, strong clinical data to justify premium pricing, patent protection, and strategic regional expansion are crucial.
Sources
[1] Regulatory filings and clinical trial registries.
[2] Competitive landscape reports from IQVIA and EvaluatePharma.
[3] Patent analysis reports from Clarivate Analytics.
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