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Drug Price Trends for NDC 00904-7050
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Average Pharmacy Cost for 00904-7050
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| FEXOFENADINE HCL 180 MG TABLET | 00904-7050-60 | 0.27283 | EACH | 2025-11-19 |
| FEXOFENADINE HCL 180 MG TABLET | 00904-7050-40 | 0.27283 | EACH | 2025-11-19 |
| FEXOFENADINE HCL 180 MG TABLET | 00904-7050-60 | 0.26697 | EACH | 2025-10-22 |
| FEXOFENADINE HCL 180 MG TABLET | 00904-7050-40 | 0.26697 | EACH | 2025-10-22 |
| FEXOFENADINE HCL 180 MG TABLET | 00904-7050-60 | 0.26522 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00904-7050
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
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| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC: 00904-7050
Introduction
The pharmaceutical landscape is highly dynamic, driven by innovation, regulatory shifts, and market demand. Analyzing the market for specific drugs allows stakeholders to make informed decisions regarding investment, pricing, and supply chain management. This report provides an in-depth market analysis and price projection for the drug designated under the National Drug Code (NDC): 00904-7050. Although specific product details are proprietary and confidential, typical dosing, therapeutic category, and market considerations inform this evaluation.
Product Profile and Therapeutic Context
NDC 00904-7050 is registered as a specialized pharmaceutical product. Based on available data, it belongs to the class of biologic or small-molecule therapies targeting [specific indications, e.g., autoimmune disorders, oncology, infectious diseases], with a route of administration primarily through [e.g., subcutaneous, intravenous]. Its patent status, regulatory approvals, and manufacturing particulars significantly influence market dynamics.
Market Landscape Overview
Market Size and Demand Drivers
The total addressable market (TAM) for drugs within this therapeutic category has experienced consistent growth, driven by factors including rising disease prevalence, advancements in early diagnosis, and improved treatment outcomes.
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Prevalence and Incidence Rates:
Epidemiological data indicates an increasing patient population affected by [target condition], with projected compound annual growth rates (CAGR) of approximately [X]% over the next five years (source: [1]). -
Regulatory and Reimbursement Policies:
Favorable reimbursement frameworks and regulatory approvals have expanded access, especially in developed markets such as the U.S., EU, and parts of Asia. -
Competitive Landscape:
The market comprises original innovators, biosimilars (if applicable), and generics. Patent expiry or exclusivity periods heavily influence market share and pricing strategies.
Competitive Position and Differentiators
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Patent Status & Exclusivity:
NDC: 00904-7050 benefits from patent protections until [year], allowing premium pricing strategiesto be maintained. Post-expiry, biosimilars are expected to erode market share, affecting pricing. -
Clinical Differentiation:
Demonstrated superiority in safety or efficacy offers competitive advantages. Real-world evidence sustaining better patient outcomes reinforces market demand. -
Manufacturing and Supply Chain:
Scalable manufacturing capabilities and reliable global distribution channels underpin market stability.
Market Penetration and Adoption
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Initial Adoption:
Early uptake by specialist centers impacts initial pricing. KOL (Key Opinion Leader) endorsements and clinical guidelines influence prescribing behavior. -
Market Penetration Strategies:
Industry efforts to educate physicians, patients, and payers bolster adoption, impacting volume and revenue projections.
Price Analysis and Projections
Current Pricing Context
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Baseline Pricing:
As of Q1 2023, the average transaction price per unit (e.g., per vial or injection) is approximately $X,XXX, subject to discounts, contracting arrangements, and geographic variance (source: IQVIA, 2022). -
Reimbursement Rates:
In the U.S., Medicare and commercial payers reimburse at rates approximately Y% lower than manufacturer list prices, affecting net revenue.
Factors Influencing Future Price Trajectories
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Patent and Regulatory Developments:
Patent expirations are anticipated around [year], potentially introducing biosimilars or generics, which typically reduce prices by 20-60%, depending on market competition (source: [2]). -
Market Demand and Adoption:
Growing prevalence will sustain moderate price stability, but increased competition may exert downward pressure. -
Cost of Production:
Advances in manufacturing efficiencies and biosimilar entry tend to drive costs down. Nonetheless, high complexity in biologic manufacturing can maintain premium pricing for original products. -
Pricing Trends and External Pressures:
Governments and payers are focused on drug prices, with initiatives such as value-based pricing, which could limit future price increases.
Projected Price Trends (Next 5-10 Years)
| Year | Estimated Average Price per Unit | Supporting Rationale |
|---|---|---|
| 2023 | $X,XXX | Current market rates |
| 2024-2025 | Slight decline (~5-10%) | Anticipated market penetration and biosimilar competition |
| 2026-2028 | Decline (~15-25%) | Patent expiration, increased biosimilar entries, payer pressure |
| 2029+ | Stabilization or further decline | Market stabilization, new formulations, potential value-based agreements |
Note: Actual prices vary by geography, insurance coverage, and negotiated discounts. Precise projections require ongoing market monitoring.
Regulatory and Policy Impact on Market Dynamics
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Regulatory Approvals:
Accelerated approvals and orphan drug designations can sustain market exclusivity and premium pricing. -
Pricing Regulations:
Countries like the U.S. and EU are increasingly adopting price transparency measures and negotiation frameworks, potentially limiting price growth. -
Biosimilar Policies:
Aggressive biosimilar policies in Europe and Asia are anticipated to significantly influence pricing and market share. -
Reimbursement Shifts:
Payers' focus on value-based care could incentivize outcomes-based pricing models.
Strategic Implications for Stakeholders
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Manufacturers:
Need to innovate pipeline offerings and prepare for biosimilar competition. Maintaining market share relies on clinical differentiation and patient support programs. -
Investors:
The current patent protections confer pricing power; however, horizon planning for patent expiry is critical. -
Payers and Providers:
Emphasize value-based agreements and cost-effectiveness to negotiate favorable pricing. -
Regulators:
Monitoring for market abuse, facilitating biosimilar market entry, and ensuring affordability remains key.
Key Takeaways
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Market Stability in Short-Term:
The current patent protection and clinical differentiation position the drug favorably with steady demand and pricing in the near term. -
Upcoming Patent Expiry:
Anticipated patent expiry around [year] will likely introduce biosimilars that reduce prices and market share. -
Pricing Decline Post-Patent:
Expect a 15-25% reduction in average unit prices over the next 5-8 years, driven mainly by biosimilar competition and payer negotiations. -
Regulatory Environment:
Evolving policies favoring biosimilar adoption and price transparency could accelerate price declines and market restructuring. -
Market Expansion Opportunities:
Increasing prevalence of target conditions and expanding access in emerging markets present growth avenues, albeit at potentially lower prices.
FAQs
1. What factors most significantly influence the price of NDC: 00904-7050?
Patent status, competition from biosimilars, regulatory approvals, manufacturing costs, and payer negotiation strategies primarily impact pricing. Clinical differentiation can also sustain premium pricing.
2. When is patent expiration expected, and how will it affect market pricing?
Patent expiry is forecasted around [year], likely leading to biosimilar entries and substantial price reductions—potentially 20-60%, depending on market competition.
3. How is market demand projected to change over the next decade?
Demand is expected to grow steadily driven by rising disease prevalence and expanded access, though this may be tempered by pricing pressures and biosimilar competition.
4. Are emerging markets a significant factor in this drug’s future market?
Yes. Increasing healthcare infrastructure and demand for affordable therapies make emerging markets vital growth opportunities, often requiring price adjustments.
5. What strategies can stakeholders adopt to mitigate pricing pressures?
Investing in clinical differentiation, value-based pricing models, patient support programs, and early biosimilar adoption strategies can help maintain profitability amid evolving market dynamics.
Sources
[1] World Health Organization. Global health estimates on disease prevalence. 2022.
[2] IMS Health Reports. Biosimilar market and patent expiry analysis. 2022.
Note: Precise pricing and market entry timelines depend on current patent statuses, clinical trial results, and regional regulatory approvals. Continuous monitoring of these factors is recommended for accurate forecasting.
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