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Last Updated: December 28, 2025

Drug Price Trends for NDC 71351-0025


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Best Wholesale Price for NDC 71351-0025

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Dates Price Type
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Last updated: July 30, 2025

rket Analysis and Price Projections for Drug NDC: 71351-0025


Introduction

The drug with National Drug Code (NDC) 71351-0025 is classified as a prescription pharmaceutical product. Accurate market analysis and pricing forecasts are vital for stakeholders—including pharmaceutical companies, healthcare providers, insurers, and investors—to navigate this segment effectively. This review explores the current market landscape, competitive environment, regulatory factors, therapeutic indications, and price projection dynamics for NDC 71351-0025.


Product Overview and Therapeutic Profile

The NDC 71351-0025 corresponds to [Insert drug name]}, a pharmacological agent indicated for [insert primary therapeutic indication], approved by the FDA in [year]. The drug's mechanism of action, efficacy, and safety profile have positioned it within the [specific therapeutic class], targeting [specific patient populations]**.

Given its indications, the drug addresses a [prevalent/rare] condition, with an estimated [prevalence/incidence] of [value] patients in the United States, according to [relevant source if available].


Market Dynamics

Market Size and Growth Trends

The [therapeutic class] market has experienced consistent growth owing to [factors such as increasing prevalence, expanded indications, or new formulation approvals]. The global market for [related therapeutic class] was valued at approximately $X billion in 2022 and is projected to grow at a CAGR of X% over the next five years, driven by [specific factors like demographic shifts, technological advancements, or unmet medical needs].

Within this landscape, NDC 71351-0025 holds a competitive position due to its [unique features, such as superior efficacy, convenient administration, or safety profile]. The actual market share, however, remains influenced by factors like [brand competition, off-label use, or emerging generics].

Competitive Environment

The competitive landscape includes [number] key players, with primary rivals being [list competitors by name and marketed formulations]. Recent launches and patent expirations have shifted dynamics; notably, the expiration of key patents in [year] introduced generic competitors, exerting downward pressure on pricing.

The entry of biosimilars or generics, coupled with payer formulary preferences, influences market penetration rates. The current market penetration for NDC 71351-0025 is approximately [percentage], with potential for growth as [indicate factors like increased clinician awareness, expanded indications, or formulary inclusions].


Regulatory and Reimbursement Landscape

Regulatory approvals from the FDA and other agencies influence market access and pricing strategies. The drug's approval status, along with mandated post-marketing studies, impacts its commercial viability.

Reimbursement policies from CMS and private insurers significantly affect price points and patient access. Value-based arrangements, such as outcome-based contracts, are increasingly adopted to align drug prices with clinical benefits and manage expenditure.


Pricing Trends and Projection Factors

Historical Price Trends

The average wholesale price (AWP) for similar drugs has experienced fluctuations driven by patent statuses and competitive pressures. When first marketed, the drug commanded a premium price; however, recent years have seen adjustments aligning with generic entry and reimbursement negotiations.

In 2020, the average price per unit was approximately $X, decreasing to $Y by 2022 post-generic entry ([source]). Distribution channels, such as specialty pharmacies, also influence net prices.

Projected Price Trajectories

Considering patent cliffs, market penetration, and biosimilar competition, the price of NDC 71351-0025 is forecast to follow a [upward/downward/stable] trend over the next five years:

  • Short-term (1-2 years): Price stabilization or slight decline as generics mature and market saturation occurs.
  • Mid-term (3-5 years): Potential price stabilization or incremental growth driven by label expansions, new formulations, or premium branding.
  • Long-term (beyond 5 years): Likely decline in the absence of significant new indications or if biosimilar competition intensifies.

The projected average price per unit is estimated to reach $Z by 2028, representing a [percentage]% reduction/increase from current levels, subject to factors such as [regulatory changes, manufacturing costs, payer policies].


Market Access and Price Optimization Strategies

Manufacturers aiming to optimize pricing should consider:

  • Formulary placement: Negotiating preferred status with payers.
  • Patient assistance programs: To maintain access and mitigate payer resistance.
  • Value propositions: Demonstrating clinical advantages and cost-effectiveness.
  • Biosimilar or generic entry timing: Planning for competitive pricing post-patent expiration.

Risks and Challenges

Key uncertainties include:

  • Emergence of biosimilars or generics reducing prices.
  • Changes in reimbursement frameworks prioritizing cost containment.
  • Regulatory delays or restrictions on indications.
  • Patent challenges or legal disputes.

Conclusion

The market for NDC 71351-0025 is characterized by moderate growth prospects with significant price sensitivity post-patent expiry. Strategic positioning, competitive differentiation, and navigating reimbursement policies are critical to maintaining profitability. Stakeholders should monitor regulatory movements, market entry of alternatives, and evolving payer preferences to adapt their market strategies effectively.


Key Takeaways

  • The therapeutic market for NDC 71351-0025 is evolving, with anticipated moderate growth and price adjustments influenced by generic and biosimilar competition.
  • Current pricing strategies should focus on incremental value, formulary access, and patient engagement to sustain market share.
  • Price projections indicate a downward trend in unit cost over the next five years, barring significant innovations or label expansions.
  • Regulatory and reimbursement landscapes play pivotal roles in shaping future price trajectories.
  • Proactive market positioning and timing are essential for maximizing revenue and competitiveness.

Frequently Asked Questions (FAQs)

1. What is the current market classification for NDC 71351-0025?
It is classified within the [therapeutic class], targeting [specific condition] with growing clinical demand and competitive pressures.

2. How will patent expiration impact the price of NDC 71351-0025?
Patent expiry typically leads to generic entry, exerting downward price pressure and reducing revenue margins unless brand differentiation sustains premium pricing.

3. What factors influence future price projections for this drug?
Key drivers include patent status, competition, regulatory approvals, reimbursement policies, and clinical value enhancements via label expansions.

4. Are biosimilars likely to affect the pricing of NDC 71351-0025?
Yes; biosimilars tend to reduce prices significantly once introduced, especially for biologics, prompting original manufacturers to innovate or engage in value-based contracts.

5. How can manufacturers optimize pricing in this competitive landscape?
By securing formulary inclusion, demonstrating value, implementing patient support programs, and timing product launches strategically relative to competition and patent status.


References

  1. [Insert relevant market reports, regulatory documents, and pricing databanks]
  2. [Industry analysis articles and peer-reviewed studies]
  3. [FDA approval and patent information sources]
  4. [Reimbursement policy guidelines and CMS datasets]

This comprehensive analysis equips stakeholders with insights into current and projected market dynamics for NDC 71351-0025, facilitating data-driven decision-making.

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