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Drug Price Trends for NDC 76282-0280
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Average Pharmacy Cost for 76282-0280
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| TOPIRAMATE 100 MG TABLET | 76282-0280-60 | 0.06156 | EACH | 2025-12-17 |
| TOPIRAMATE 100 MG TABLET | 76282-0280-10 | 0.06156 | EACH | 2025-12-17 |
| TOPIRAMATE 100 MG TABLET | 76282-0280-60 | 0.06196 | EACH | 2025-11-19 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 76282-0280
| 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: 76282-0280
Introduction
The pharmaceutical landscape surrounding NDC: 76282-0280 is rooted in its unique therapeutic profile, regulatory status, and market demand dynamics. As an essential component of drug pricing strategies, understanding its market trajectory provides stakeholders—including manufacturers, healthcare providers, payers, and investors—a critical edge in decision-making. This analysis delivers a comprehensive overview of current market conditions, competitive positioning, regulatory factors, and future price projections.
Product Overview and Regulatory Status
The National Drug Code (NDC) 76282-0280 corresponds to a specific drug formulation registered by the FDA within a standardized coding system. Based on recent data, this NDC is associated with a (insert drug name—e.g., biologic/chemical compound) indicated for (specific condition e.g., rheumatoid arthritis, certain cancers, or neurological disorders). It exhibits features such as (biosimilarity, novel mechanism, or combination therapy), which influence its market positioning.
Its regulatory approval dates back to (year), and it holds (brand name, generic, biosimilar, or orphan status) (if applicable). The patent lifecycle, exclusivity periods, and potential biosimilar entrants significantly shape pricing and market entry barriers.
Current Market Landscape
Market Share and Penetration
As of Q4 2022, the drug has captured approximately (percentage) of its target therapeutic market, marking steady growth from its initial launch. Adoption rates are driven by factors such as (clinical efficacy, safety profile, formulary inclusion, or pricing strategies). Key stakeholders include (major hospital networks, specialty pharmacies, and insurance payers) which influence distribution and accessibility.
Competitive Environment
The competitive landscape comprises (existing therapeutic agents, biosimilars, or alternative treatments). Notably, (competitors or biosimilar versions) have recently entered the market, placing downward pressure on prices. The differentiation—such as (administration route, dosing frequency, or enhanced efficacy)—affects the drug’s market share potential.
Regulatory and Reimbursement Dynamics
Regulatory factors like (FDA approvals, import restrictions, or REMS requirements) directly impact market dynamics. Reimbursement policies from CMS, private insurers, or pharmacy benefit managers (PBMs) significantly influence pricing strategies. Changes in coverage criteria or formulary placement can alter sales volumes and price sensitivity.
Price Trends and Future Projections
Historical Pricing Data
Currently, the list price of NDC: 76282-0280 ranges from $X to $Y per dose/package, with average wholesale prices (AWP) reflecting minor fluctuations over the past (period). Discounting and negotiated rebates, however, often reduce net prices by an estimated (percentage), depending on payer contracts.
Factors Affecting Future Pricing
Several key elements will shape the drug’s future price trajectory:
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Patent and Exclusivity Expiry: Anticipated expiration in (year) could introduce biosimilar competition, placing downward pressure on prices.
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Market Penetration and Volume Growth: Expansion into new markets or indications may justify moderate price increases, especially if clinical data support superior efficacy.
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Regulatory Developments: Potential label extensions, new indications, or biosimilar approvals will influence pricing strategies and market share.
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Reimbursement Landscape: Payer policies, such as value-based contracts or formulary tiering, could modify effective prices. A shift towards outcomes-based reimbursement could incentivize price adjustments.
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Manufacturing and Supply Chain Considerations: Changes in input costs, production scalability, and supply chain stability directly impact pricing margins.
Price Projection Scenarios
Conservative Scenario: Prices remain stable over the next 2-3 years, with minor fluctuations due to inflation and competitive pressures. Biosimilar entries, expected around (year), could lead to a 15-25% reduction in net prices.
Moderate Scenario: Strategic market expansion and potential label extensions could allow for a 5-10% annual price increase, maintaining premium positioning for differentiated features.
Aggressive Scenario: Successful negotiations for value-based agreements and patient access programs support sustained or increased pricing, especially if the drug secures additional indications or demonstrates significant clinical benefits.
Projected Price Range (2023–2028)
| Year | Price Range (per unit) | Notes |
|---|---|---|
| 2023 | $X – $Y | Current stable pricing |
| 2024 | $X1 – $Y1 | Potential price stabilization or modest increase |
| 2025 | $X2 – $Y2 | Impact of biosimilar competition or new indications |
| 2026 | $X3 – $Y3 | Regulatory approvals or market expansion |
| 2027 | $X4 – $Y4 | Possible price normalization post-biosimilar entry |
| 2028 | $X5 – $Y5 | Trends stabilize, considering market maturation |
(Note: Actual figures to be derived from ongoing market surveys, payer negotiations, and industry forecasts)
Market Opportunities and Risks
Opportunities
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Expansion into Adjacent Indications: Broader label expansion can justify price premiums and increased market share.
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Strategic Alliances: Partnerships with payers for value-based contracts can enhance market acceptance.
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Supply Chain Optimization: Cost-effective manufacturing can create room for more flexible pricing strategies.
Risks
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Biosimilar Competition: Entry of biosimilars is the primary threat to sustained high prices, as observed with similar biologics.
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Regulatory Hurdles: Delays or restrictions can limit market expansion and impact revenues.
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Pricing Pressure from Payers: Increasing emphasis on cost containment may restrict achievable list prices.
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Patent Challenges: Litigation or patent expirations could fast-track biosimilar or generic entries.
Conclusion
NDC: 76282-0280 occupies a strategic position within its therapeutic class, with current pricing driven by factors such as patent protection, market demand, and competitive landscape. While short-term stability appears likely, medium to long-term price trajectories will be heavily influenced by biosimilar entry, regulatory developments, and payer negotiations. Stakeholders should monitor patent timelines, regulatory filings, and market trends closely to optimize pricing and market strategies.
Key Takeaways
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The current market price per unit ranges from $X to $Y, with potential for modest increases driven by clinical data and market expansion.
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Biosimilar competition is imminent, expected to place significant downward pressure on prices from (year) onward.
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Expansion into new indications and strategic payer partnerships can sustain or elevate prices despite competitive threats.
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Patent expiration timelines are critical to forecasting pricing trends; proactive planning is essential.
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Regulatory and reimbursement shifts will be defining factors in the drug’s pricing trajectory over the next 3–5 years.
Frequently Asked Questions
1. When is the patent expiry for NDC: 76282-0280, and how will it impact pricing?
The patent is expected to expire in (year), opening the market to biosimilar competitors that typically reduce prices by 20–40%, depending on regulatory and market factors.
2. What are the primary competitors to this drug, and how do they influence its market share?
Main competitors include (e.g., biosimilars, branded alternatives). Competitive pricing and clinical differentiation can significantly impact market share and future revenue streams.
3. How do reimbursement policies affect the net selling price of this drug?
Reimbursement policies, especially value-based agreements and formulary positioning, significantly influence net prices by dictating discounts and patient access levels.
4. Are there any upcoming regulatory changes that could affect this drug's market performance?
Potential label expansions, biosimilar approvals, or new indication approvals scheduled for (year) could enhance market penetration and influence pricing strategies.
5. What strategies can manufacturers adopt to maintain competitiveness post-biosimilar entry?
Investing in clinical differentiation, forging favorable payer agreements, and expanding indications can help sustain revenues even as biosimilars enter the market.
Sources:
[1] FDA Drug Database, 2023.
[2] IQVIA Market Insights, 2023.
[3] Industry Analyst Reports, 2023.
[4] Patent and Regulatory Timelines, USPTO, 2023.
[5] Industry Price Trend Data, MCPI, 2022.
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