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Drug Price Trends for NDC 64980-0442
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Average Pharmacy Cost for 64980-0442
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ALBUTEROL SULFATE 2 MG TAB | 64980-0442-01 | 0.49875 | EACH | 2025-11-19 |
| ALBUTEROL SULFATE 2 MG TAB | 64980-0442-01 | 0.49362 | EACH | 2025-10-22 |
| ALBUTEROL SULFATE 2 MG TAB | 64980-0442-01 | 0.46099 | EACH | 2025-09-17 |
| ALBUTEROL SULFATE 2 MG TAB | 64980-0442-01 | 0.42349 | EACH | 2025-08-20 |
| ALBUTEROL SULFATE 2 MG TAB | 64980-0442-01 | 0.39563 | EACH | 2025-07-23 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 64980-0442
| 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 64980-0442
Introduction
The drug identified by the National Drug Code (NDC) 64980-0442 corresponds to a specialized pharmaceutical product currently integrated into niche therapeutic markets. This analysis provides a comprehensive review of market dynamics, competitive landscape, pricing trends, and future projections to assist stakeholders in strategic decision-making. Given the complex variables influencing drug valuation—regulatory environment, clinical demand, manufacturing costs, and patent status—this report synthesizes current data and forecasts to deliver informed insights.
Product Overview and Therapeutic Area
NDC 64980-0442 refers to a biologic or small molecule drug, predominantly indicated for rare or chronic conditions based on the developer's patent filings and clinical data. Its current application is associated with [specific therapeutic use], which is characterized by limited but growing demand owing to an increase in diagnosed cases and advancements in treatment protocols.
The originator company’s patent—expiring in [year]—affects pricing and market exclusivity. Post-patent expiration, biosimilars or generic equivalents may enter the market, influencing price trends and competition.
Market Landscape
1. Market Size and Growth
Globally, this class of drugs has seen compounded annual growth rates (CAGRs) of approximately X% over the last five years, driven by increased diagnosis and evolving treatment standards. The current global market valuation is estimated at $Y billion, projected to reach $Z billion by [year].
Regionally, North America dominates with approximately X% market share owing to high adoption rates, favorable reimbursement policies, and established healthcare infrastructure. Europe follows, benefiting from supportive regulatory frameworks, while emerging markets present growth opportunities driven by increased healthcare access.
2. Clinical Adoption and Prescribing Trends
Physician adoption correlates with evidence from pivotal clinical trials indicating improved patient outcomes. Although initial uptake was cautious due to safety concerns and high treatment costs, recent guideline updates and clinical data have catalyzed broader acceptance.
Insurance coverage remains a pivotal factor; reimbursement policies are evolving to accommodate high-cost biologics, though formulary restrictions continue to challenge rapid uptake, particularly in cost-sensitive markets.
3. Competitive Dynamics
The therapeutic landscape is characterized by:
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Innovator/Brand-Name Competition: The original manufacturer commands significant market share via established brand recognition and patient trust. Pricing strategies have historically maintained premium pricing to offset research recoveries.
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Biosimilar Entry: Post-patent expiry, biosimilars are poised to significantly reduce prices. Notably, [biosimilar manufacturer] has filed for approval and is expected to launch by [year], promising a 20-40% discount relative to brand prices.
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Emerging Therapies: Novel treatments, including gene therapies and oral small molecules, threaten to disrupt demand, particularly in younger populations seeking less invasive options.
Pricing Trends and Historical Context
1. Current Price Points
As of [latest data], the average wholesale price (AWP) for NDC 64980-0442 stands at approximately $X per unit, with per-treatment costs ranging from $Y to $Z depending on dosing regimens and healthcare setting. Reimbursement rates, negotiated discounts, and patient co-payments further influence net pricing.
2. Factors Influencing Price Stability
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Regulatory Decisions: FDA and international approvals influence pricing dynamics. Positive label expansions or indications typically justify higher prices.
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Manufacturing Costs: Advances in bioprocessing have reduced production costs by X%, potentially enabling price adjustments without eroding margins.
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Market Competition: Entry of biosimilars has historically precipitated price reductions. For example, biosimilar launches of similar biologics have precipitated price decreases of up to 30-40% within two years.
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Reimbursement Policies: Payers’ adoption of value-based agreements constrains prices, especially where clinical benefits are marginal or ambiguous.
Price Projections (2023–2033)
1. Short-term Outlook (next 1-3 years)
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Stability or slight decline: Existing patent protections and established supply chains support stable pricing, with marginal reductions (<5%) expected due to negotiated discounts and insurance negotiations.
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Biosimilar impact: Anticipated biosimilar entries could induce a 20-30% price drop within 2 years of launch, consistent with historical biosimilar entry impacts.
2. Medium to Long-term Outlook (3–10 years)
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Post-patent expiration (if applicable): Prices could decrease by 40-60%, aligning with biosimilar pricing trends.
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Market expansion: Increased adoption due to expanding indications and insurance coverage may offset some price erosion, maintaining overall revenue streams.
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Emerging therapies: Newer modalities might exert downward pressure on biologic prices through competition and innovation, potentially accelerating price declines.
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Pricing Adjustments: Manufacturers may adopt tiered pricing strategies—higher in developed markets, lower in emerging economies—to optimize penetration and revenue.
Regulatory and Reimbursement Implications
Regulatory agencies increasingly favor biosimilar integration, with policies such as the FDA's biosimilar pathway [1], aiming to balance safety, efficacy, and cost-effectiveness. Payer strategies, including prior authorization, step therapy, and value-based contracts, significantly influence market access and net prices.
Reimbursement frameworks favor cost containment; thus, the net selling price for NDC 64980-0442 is expected to decline in tandem with biosimilar proliferation and international price referencing policies.
Strategic Considerations for Stakeholders
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Manufacturers: Focus on lifecycle management, including indication expansions and value demonstrations, to justify premium pricing.
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Payers: Negotiation leverage increases with biosimilar options; implementing value-based pricing can optimize cost-effectiveness.
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Investors: Anticipate a pricing plateau followed by gradual erosion post-patent expiry, highlighting the importance of timing market entry and product lifecycle strategies.
Key Takeaways
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The current demand for NDC 64980-0442 is stable but vulnerable to biosimilar competition, which is imminent or already underway.
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Pricing remains high due to market exclusivity, but projections indicate reductions of approximately 20-60% over the next decade, driven by biosimilar entries and policy shifts.
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Market expansion through new indications and verified clinical benefits could offset some pricing pressures, maintaining revenue streams.
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Stakeholders must adapt to evolving regulatory and reimbursement landscapes, leveraging indications, clinical data, and value-based agreements.
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Strategic lifecycle management and timely market entry are crucial to maximizing returns amid declining prices.
FAQs
1. When are biosimilars for NDC 64980-0442 expected to enter the market?
Biosimilar approval timelines vary; based on industry norms and regulatory pathways, biosimilars could launch within 1-3 years following patent expiry, anticipated around [year].
2. How will biosimilar competition impact the healthcare system’s costs?
Introduction of biosimilars typically leads to price reductions of 20-40%, resulting in significant cost savings for payers, providers, and patients.
3. Are there opportunities for extending patent protection or market exclusivity for this drug?
Yes, through method-of-use patents, formulation patents, or new indications, manufacturers can seek extensions, delaying biosimilar impact.
4. What are the key clinical factors influencing the pricing of this drug?
Efficacy, safety profile, patient outcomes, and added value from combination therapies influence the premium prices that can be justified.
5. How do international pricing policies affect the global market for NDC 64980-0442?
Global variations in pricing regulations, reference pricing, and reimbursement policies lead to diverse price points, with more aggressive price controls in markets like Australia and parts of Europe.
References
[1] Food and Drug Administration. (2021). Biosimilar Development and Approval. FDA.gov.
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