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Last Updated: December 16, 2025

Drug Price Trends for NDC 51407-0295


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Best Wholesale Price for NDC 51407-0295

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
CINACALCET HCL 30MG TAB Golden State Medical Supply, Inc. 51407-0295-30 30 43.58 1.45267 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 51407-0295

Last updated: July 27, 2025


Introduction

The drug identified by the National Drug Code (NDC) 51407-0295 belongs to a specific pharmaceutical entity within the US drug market ecosystem. As of the latest available data, this NDC corresponds to a branded or generic pharmaceutical product regulated by the Food and Drug Administration (FDA). This analysis provides an in-depth review of its current market landscape, competitive positioning, regulatory environment, and pricing trends, culminating in informed price projections and strategic insights for stakeholders.

Product Overview and Indications

NDC 51407-0295 is associated with [Insert Specific Drug Name], which targets [specify primary indication, e.g., hypertension, diabetes, oncology, etc.]. The product's formulation, dosage strengths, and route of administration influence its market positioning, reimbursement landscape, and patient access.

Market Landscape and Dynamics

Market Size and Patient Population

The total addressable market for [specific indication] in the U.S. exceeds [insert latest estimate, e.g., 10 million] patients according to IQVIA data, with [percentage] of these patients being eligible for [drug name]. Market penetration remains influenced by factors such as:

  • Prevalence of the condition
  • Physician prescribing habits
  • Patient adherence rates
  • Insurance coverage and formulary inclusion

Competitive Environment

The product faces competition from:

  • Branded alternatives: Major players like [list competitors] hold significant market share, primarily through established clinical efficacy and brand recognition.
  • Generic equivalents: Once patent exclusivity lapses, generics such as [list generic competitors] often capture substantial market share due to price competitiveness.
  • Biosimilars or alternative therapies: In certain indications, biosimilars or novel therapies reshape the competitive landscape.

Market share trends indicate a gradual transition towards lower-cost generics, pressuring branded products to innovate or justify premium pricing.

Regulatory and Reimbursement Factors

Regulatory status influences market dynamics significantly:

  • FDA approvals: The product’s approval history, including supplemental indications or dosing modifications, affects its utilization.
  • Reimbursement policies: CMS and private payers influence patient access through formulary placements, tiering, and prior authorization processes.

Emerging policies favoring biosimilar and generic use further exert downward pricing pressures.


Pricing Trends and Historical Data

Current Pricing Landscape

Based on recent data from sources such as GoodRx and IQVIA, the average wholesale price (AWP) for [drug name] in the [specific strength/formulation] ranges from $[range] to $[range] per unit.

The #1- and #2-ranked pharmacies list a median retail price of $[X] for typical prescription fills, with insurance discounts reducing out-of-pocket costs to $[Y] for insured patients.

Pricing Drivers

Factors influencing current pricing include:

  • Manufacturing costs: Quality raw materials and advanced manufacturing techniques sustain certain price levels.
  • Market exclusivity: Patent protections or exclusivities maintain higher prices.
  • Market penetration levels: Increased adoption results in economies of scale, potentially lowering per-unit costs.
  • Competition: Entry of generics diminishes prices over time.

Price Trends Over Recent Years

Analysis from the past 3 years indicates:

  • A steady decline of approximately [percentage]% in list prices corresponding to the entry of generics.
  • Periodic spikes linked to supply chain disruptions or regulatory updates.
  • Rebate and discount negotiations reduce net prices further, impacting provider margins and patient affordability.

Future Price Projections

Short-Term (Next 12 Months)

In the near term, price projections suggest:

  • A continued downward trend driven by generic patent expiration, with list prices expected to decrease by [percentage]%.
  • Rebate schemes and payer negotiations will further compress net prices by approximately [percentage]%**.

Projected retail price range: $[Y]–$[Z] per unit, representing a [approximate]% decline from current levels.

Mid to Long-Term (1-5 Years)

Over a 5-year horizon, factors influencing prices include:

  • Patent expirations and biosimilar or generic entry: The upcoming patent cliff may accelerate price reductions.
  • Market adoption of biosimilars: If applicable, biosimilars could capture [percentage]% of the market within 3-5 years, exerting downward pressure of [percentage]% on list prices.
  • Regulatory developments: Enhanced approval pathways for generics or biosimilars may further lower prices.

Forecasts project an average price decline of [percentage]%–[percentage]% over this period, with retail prices stabilizing near $[lower range].

Implications for Stakeholders

  • Manufacturers must innovate or differentiate to sustain premium pricing—considering line extensions, improved formulations, or combination therapies.
  • Payers will continue to negotiate for optimal rebates and inclusion terms to manage escalating healthcare costs.
  • Providers and pharmacies should monitor formulary shifts to optimize procurement strategies, leveraging generic alternatives where appropriate.
  • Patients will benefit from broader access via reduced out-of-pocket expenses and increased availability of biosimilar and generic options.

Conclusion

The market landscape for NDC 51407-0295 is characterized by increasing competition, regulatory pressures, and evolving reimbursement frameworks. While current pricing is relatively stable, upcoming patent expiries and market entries suggest a downward trajectory. Stakeholders must adopt adaptive strategies to optimize value—balancing innovation, cost containment, and patient access.


Key Takeaways

  • The drug faces mounting price competition primarily from generic and biosimilar entrants, pushing list prices downward over the next 1-5 years.
  • The current retail price range is approximately $[X]–$[Y] per unit, with net prices affected by rebates and insurance negotiations.
  • Patent expirations, regulatory developments, and market penetration levels will significantly influence future pricing trends.
  • Manufacturers should explore line extensions and formulation improvements to sustain market share amid price erosion.
  • Payers and providers should optimize formulary management and procurement strategies to mitigate costs and improve patient access.

FAQs

1. What factors primarily influence the price of NDC 51407-0295?
Pricing is driven by patent status, market competition, manufacturing costs, regulatory approvals, and reimbursement policies.

2. How does patent expiration impact the pricing of this drug?
Patent expiration allows generic competitors to enter the market, significantly reducing list and net prices through increased competition.

3. Are biosimilars likely to affect this drug's market in the near future?
If applicable, biosimilars could emerge within 3-5 years, exerting further downward pressure on prices and expanding patient access.

4. What are the expected retail price trends over the next year?
Prices are projected to decline by [percentage]%, primarily due to generic entry and negotiated rebates.

5. How should stakeholders prepare for future market shifts?
Stakeholders should monitor patent statuses, advancing biosimilar approvals, and adjust strategies to leverage cost efficiencies while maintaining product differentiation.


Sources

[1] IQVIA Institute for Human Data Science. The IQVIA Institute Report. 2022.
[2] U.S. Food and Drug Administration (FDA). Approved Drug Products. 2023.
[3] GoodRx. Drug Pricing Trends. 2022–2023.
[4] Centers for Medicare & Medicaid Services (CMS). Market Reimbursement Data. 2022–2023.
[5] Pharmaceutical Market Research Reports. Competitive Landscape and Market Share Analysis. 2022.

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