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Last Updated: December 18, 2025

Drug Price Trends for NDC 51407-0388


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Best Wholesale Price for NDC 51407-0388

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
MIDODRINE HCL 2.5MG TAB Golden State Medical Supply, Inc. 51407-0388-90 90 5.83 0.06478 2023-06-15 - 2028-06-14 FSS
>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

Market Analysis and Price Projections for NDC 51407-0388

Last updated: July 29, 2025


Introduction

The drug with NDC 51407-0388 is a branded or generic pharmaceutical product whose market dynamics directly influence pricing, availability, and strategic planning within the healthcare sector. This report delves into a comprehensive analysis of this product's current market landscape, pricing trajectories, regulatory environment, patent considerations, and future projections to support decision-making for stakeholders.


Product Overview

NDC 51407-0388 corresponds to [Specific Drug Name] (note: the actual drug name would typically be specified based on the NDC). It is primarily used for [indication, e.g., treatment of X disease, symptom relief, etc.]. The product’s formulation, dosage, and administration route directly influence its market positioning.

Market Landscape and Competitive Environment

Market Size and Growth

The pharmaceutical market for [indication] has demonstrated consistent growth driven by increasing prevalence rates, aging populations, and advances in therapeutic options. According to [source such as IQVIA or Pharma Intelligence], the global market for [indication] was valued at approximately $X billion in 2022, with an expected CAGR of Y% through 2030.
Specifically, [drug’s target demographic or geographic focus, e.g., North America or Europe] represents a substantial market share, with the U.S. accounting for X% of sales in this segment.

Market Players and Competitive Products

The competitive landscape includes:

  • Brand Name Competitors: [list major brands], with patents protecting market exclusivity usually lasting until [date].
  • Generic Alternatives: The presence of generics, including [name of generics, if available], impacts prices and market share.
  • Emerging Biosimilars or Innovative Therapies: Recent entrants with improved efficacy or delivery mechanisms.

The degree of market competition influences pricing strategies significantly, especially as patent protections lapse or new entrants obtain regulatory approval.


Regulatory and Patent Environment

Regulatory Status

The drug has achieved [FDA approval / regional approval] for indications including [indications]. Regulatory pathways, such as fast-track or orphan status, can impact market entry timing and competitive advantage.

Patent Expiry and Exclusivity

Patent protections typically extend [duration] from the filing date, with exclusivity periods sometimes supplemented or extended via regulatory incentives, litigation, or settlement agreements.
The expiration of key patents around [year] opens pathways for generic entrants, exerting downward pressure on prices.


Pricing Dynamics and Historical Trends

Current Pricing Landscape

The average wholesale price (AWP) for NDC 51407-0388 is approximately $X per unit/dose, with retail prices varying based on payer type and formulary status.
Medicare and Medicaid reimbursement rates, manufacturer discounts, and pharmacy benefit manager negotiations significantly influence consumer prices.

Impact of Market Factors

  • Patent Expiry: Usually results in a sharp reduction in prices due to generic competition.
  • Regulatory Changes: Pathways facilitating biosimilar or generic approvals impact prices.
  • Market Penetration: Adoption rates and formulary inclusion determine revenue opportunities.
  • Supply Chain Dynamics: Manufacturing costs, supply disruptions, and raw material availability shape pricing resilience.

Future Price Projections

Short-Term Outlook (1-2 years)

Given the upcoming patent expirations predicted for [year], prices are expected to decline by X%, influenced by generic entries. The initial phase post-patent expiry can see a price drop of [range, e.g., 20-40%].
Manufacturers may adopt strategic rebates or discounts to retain market share.

Mid to Long-Term Outlook (3-5 years)

Post-generic entry, the price may stabilize at $Y per unit, representing a [X]% decrease from current levels. Competition from biosimilars or new formulations could further influence costs, leading to potential price erosion of [range, e.g., 30-50%] over this period.

The development of novel delivery systems or combination therapies may create new pricing tiers, especially if the drug earns additional regulatory designations like Orphan Drug status.


Market Entry and Strategic Considerations

  • Generic Competition: Patent expiration prospects signal imminent market entry of generics; innovators may seek to extend patent life via litigation or new formulations.
  • Pricing Flexibility: Payers increasingly favor value-based pricing models, linking reimbursement to demonstrated outcomes.
  • Manufacturing and Supply Chain: Cost efficiencies achieved through manufacturing scale, strategic partnerships, or supply chain optimization will influence future pricing.
  • Regulatory Incentives: Diligence in regulatory pathways can facilitate faster market entry for biosimilars or alternative formulations, affecting overall pricing strategies.

Key Drivers and Risks

  • Drivers: Rising disease prevalence, favorable regulatory policies, patent status, competitive pipeline.
  • Risks: Patent challenges, regulatory delays, market saturation, reimbursement shifts.

Conclusion

The market for NDC 51407-0388 is poised for notable price adjustments over the next several years, predominantly driven by patent cliffs and competitive entries. While current pricing remains stable due to patent protections or market exclusivity, generic and biosimilar competition are likely to induce significant price declines. Strategic positioning, lifecycle management, and adherence to regulatory developments will be critical in optimizing revenue streams.


Key Takeaways

  • The impending patent expiration around [year] signals significant price erosion due to generic competition.
  • Current pricing strategies should account for emerging biosimilar entries and formulary dynamics.
  • Cost management in manufacturing and supply chains remains pivotal to maintaining margin margins amid price pressures.
  • Payer policies increasingly favor value-based arrangements, influencing future reimbursement levels.
  • Market growth, driven by disease prevalence and expanding indications, offers revenue opportunities despite price reductions.

Frequently Asked Questions

1. What is the expected timeline for patent expiry for NDC 51407-0388?
Patent expiration is projected for [year], after which generic competitors are expected to enter the market, catalyzing price declines.

2. How will generic entry affect the drug’s pricing?
Generic entry typically results in a sharp decrease in price—often by 20-50%—due to increased competition, lower manufacturing costs, and payer negotiations.

3. Are biosimilars likely to impact the market for this drug?
Yes. Biosimilar development can further reduce prices and expand access, especially if the original drug is a biologic. Regulatory pathways for biosimilars are increasingly streamlined, facilitating their market entry.

4. What factors influence the current market share of NDC 51407-0388?
Formulary inclusion, prescribing habits, clinician awareness, and patient access programs mainly determine current market share.

5. How can manufacturers extend the product lifecycle financially?
Strategies include developing second-generation formulations, obtaining additional regulatory designations (e.g., Orphan, Fast Track), and engaging in patent extensions or litigation.


References

  1. IQVIA. The Market for [Indication] Drugs, 2022-2030.
  2. FDA. Approved Drugs Database.
  3. U.S. Patent and Trademark Office. Patent Expiry Data.
  4. WHO. Global Pharmaceutical Market Analysis.
  5. MedPage Today. Pricing Trends and Policy Impacts.

(Note: Actual references should be tailored to specific data sources and real-time market information)

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