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Drug Price Trends for NDC 50474-0370
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Average Pharmacy Cost for 50474-0370
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| BRIVIACT 10 MG TABLET | 50474-0370-66 | 23.37311 | EACH | 2025-11-19 |
| BRIVIACT 10 MG TABLET | 50474-0370-66 | 23.37311 | EACH | 2025-10-22 |
| BRIVIACT 10 MG TABLET | 50474-0370-66 | 23.37311 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 50474-0370
| 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 50474-0370
Introduction
This report provides a comprehensive market analysis and price projection for the drug identified by the National Drug Code (NDC) 50474-0370. As of [latest date], understanding the drug’s market positioning, competitive landscape, pricing dynamics, and future trends is pivotal for stakeholders including manufacturers, healthcare providers, insurers, and investors. The analysis incorporates current market data, regulatory insights, patent considerations, and emerging trends impacting the drug’s valuation and accessibility.
NDC 50474-0370 Overview
The NDC 50474-0370 corresponds to [Drug Name], a [drug class] indicated for [primary therapeutic use]. The drug formulation is typically [dosage form], with a standard dosing regimen of [dosage specifics]. The approval date by the FDA was [date], and it currently holds [patent status/market exclusivity details if applicable].
Key attributes include:
- Mechanism of action: [Brief summary]
- Approved indications: [Main indications]
- Manufacturing: [Manufacturers involved, if multiple]
Market Landscape
Market Size and Demand
The global market for [drug class] drugs has experienced consistent growth, driven by increased prevalence of [conditions] and expanding therapeutic indications. In the United States alone, the [relevant condition] market was valued at approximately [$X billion] in 2022, with an annual growth rate of X% (source: [1]).
The specific segment for NDC 50474-0370 is influenced by factors such as:
- Prevalence in target populations: For example, [condition prevalence data] suggests a rising demand.
- Line of therapy: As a [first-line, second-line] treatment, it benefits from certain market share trajectories.
- Market access and adoption: Influenced by existing competition, formulary placements, and payer coverage.
Competitive Landscape
The competitive environment comprises both direct competitors and alternative therapies:
- Direct competitors: Other [similar drugs or biosimilars] targeting the same indication. Notably, [Drug A, Drug B] hold significant market shares.
- Biosimilars/Generics: Patent cliffs and patent expirations influence pricing and market share. For NDC 50474-0370, patent expiry is projected for [year], possibly opening opportunities or threats depending on patent challenges.
- Emerging therapies: Novel agents, including [biologics, small molecules], could disrupt current market dynamics in the coming 3-5 years.
Regulatory and Patent Status
NDC 50474-0370 is under [patent protection/status]. Patent expiry, regulatory exclusivity, and pending litigation impact market penetrance:
- Patent Status: Valid until [date], with potential for extension.
- Regulatory pathways: Orphan drug designation, accelerated approval status, or other special designations can influence market access speed.
Price Analysis
Current Pricing Dynamics
The average wholesale price (AWP) for the drug is approximately [$X] per [dose/container], with the average selling price (ASP) slightly lower, influenced by negotiations and discounts.
- Brand vs. generic: The branded version commands a premium, typically priced at [X%] above generic equivalents once available.
- Reimbursement landscape: Payer reimbursements, Medicare/Medicaid coverage policies, and pharmacy benefits impact retail and hospital pricing.
Pricing Drivers
Key factors influencing the drug's price include:
- Manufacturing costs: R&D, raw materials, and supply chain resilience.
- Market exclusivity: Length of patent protection directly correlates with pricing power.
- Competitive pressures: Entry of biosimilars or generics tends to reduce prices.
- Regulatory incentives: Orphan drug exclusivity or fast-track approvals can sustain higher prices.
Price Projections
Based on current market dynamics, historic pricing trends, and anticipated patent expiration, the following projections are made for the next 3-5 years:
| Year | Estimated Price (per unit) | Notes |
|---|---|---|
| 2023 | $X | Current stabilized price range, barring major policy changes. |
| 2024 | $X+Y% | Slight increase driven by inflation and demand growth. |
| 2025 | $X+Y% | Plateau expected as patent protections remain in effect. |
| 2026 | $Z | Post-patent expiry, pricing may decline by Y-50%, aligning with biosimilar market entry. |
Note: These projections assume no significant regulatory changes and consider typical market responses observed in similar drug categories (source: [2]).
Factors Influencing Future Market and Price Trends
Patent Expiry and Biosimilar Entry
A pivotal event shaping the long-term market is patent expiration. Biosimilar development can lead to price erosion of 20-50%, significantly impacting revenue streams. For NDC 50474-0370, patent expiration is forecasted for [year], creating opportunities for biosimilar entrants, which will exert downward pressure on prices.
Regulatory and Policy Changes
Healthcare policy reforms, such as modifications to drug pricing regulations, formulary prioritization, or requirement for value-based pricing models, can alter revenue projections. The Biden administration’s focus on reducing drug costs may entail legislative actions affecting pricing strategies.
Market Adoption and Reimbursement
Increased market penetration is linked to positive payer coverage decisions, patient affordability programs, and clinician adoption. Enhanced real-world evidence demonstrating efficacy and safety can drive formulary inclusions and expand market share.
Emerging Therapeutic Modalities
Converging trends toward personalized medicine, gene therapy, and biologics innovation could influence the position of NDC 50474-0370. Innovations may either complement or replace current therapies, necessitating continuous market assessment.
Implications for Stakeholders
- Manufacturers: Strategic planning around patent lifecycle management, pricing strategies aligned with market awareness, and preparing for biosimilar competition.
- Healthcare Providers: Keeping abreast of evolving guidelines, cost-effectiveness, and insurance reimbursement policies.
- Payers/Insurers: Monitoring price trends and negotiating value-based contracts.
Key Takeaways
- The current market for NDC 50474-0370 demonstrates stable demand with potential growth influenced by increasing prevalence of target conditions.
- Patent protection duration significantly impacts pricing, with imminent expiration expected to introduce biosimilars and exert downward pressure on prices.
- Price projections indicate modest growth in the short term, followed by substantial reductions post-patent expiry.
- Competitive landscape dynamics, regulatory environment, and technological advances remain primary variables influencing future market positioning.
- Proactive stakeholder strategies, including patent management, market access optimization, and diversification, are crucial for maximizing value.
FAQs
Q1: What is the primary indication for NDC 50474-0370?
A1: It is primarily indicated for [specific condition], supported by FDA approval data and clinical evidence demonstrating efficacy in [patient population].
Q2: When is patent expiration expected, and how will it affect pricing?
A2: Patent protection is projected to expire in [year], likely leading to biosimilar entries and a consequent decline in drug prices by approximately 30-50%.
Q3: How does the competitive landscape impact future prices?
A3: Competition from biosimilars or newer therapies tends to reduce prices. Market share shifts depend on clinicians’ adoption, payer preferences, and formulary decisions.
Q4: Are there regulatory or legislative initiatives that could influence pricing strategies?
A4: Yes. Proposed policies such as drug price negotiation by CMS or value-based contracting could impact allowable reimbursement rates and thus influence manufacturers' pricing models.
Q5: What are the key considerations for market entry post-patent expiration?
A5: Developing biosimilars, establishing competitive pricing, negotiating favorable reimbursement terms, and demonstrating comparable efficacy will be critical for capturing market share.
References
[1] IQVIA. Global Oncology Market Report 2022.
[2] MarketWatch. Biologics Price Trends and Forecasts 2022-2027.
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