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Last Updated: December 30, 2025

Drug Price Trends for NDC 00228-2896


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Average Pharmacy Cost for 00228-2896

Drug Name NDC Price/Unit ($) Unit Date
DOXYCYCLINE HYC DR 100 MG TAB 00228-2896-11 1.79001 EACH 2025-12-17
DOXYCYCLINE HYC DR 100 MG TAB 00228-2896-11 1.78219 EACH 2025-11-19
DOXYCYCLINE HYC DR 100 MG TAB 00228-2896-11 1.86638 EACH 2025-10-22
DOXYCYCLINE HYC DR 100 MG TAB 00228-2896-11 1.95849 EACH 2025-09-17
DOXYCYCLINE HYC DR 100 MG TAB 00228-2896-11 1.96969 EACH 2025-08-20
DOXYCYCLINE HYC DR 100 MG TAB 00228-2896-11 1.93808 EACH 2025-07-23
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 00228-2896

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

Market Analysis and Price Projections for NDC 00228-2896

Last updated: August 3, 2025


Introduction

The drug identified by the National Drug Code (NDC) 00228-2896 is a critical pharmaceutical product currently integrated within multiple healthcare settings. Precise analysis of its market trajectory, competitive landscape, and price dynamics offers pivotal insights for stakeholders such as healthcare providers, manufacturers, investors, and policymakers. This briefing synthesizes current market data, historical price trends, regulatory influences, and emerging factors shaping the future pricing and demand for this medication.


Product Overview and Indications

NDC 00228-2896 corresponds to [specific drug name], formulated for [indications, e.g., treatment of [disease], prophylactic use, etc.]. Its established efficacy, safety profile, and regulatory approvals contribute to its adoption across hospitals, outpatient clinics, and specialty pharmacies. The drug’s patent protections and exclusivity periods significantly influence its market control and pricing strategies.


Current Market Landscape

Market Size and Demand Trends

The demand for NDC 00228-2896 aligns with the prevalence of its target condition. For example, if the drug addresses a chronic disease such as rheumatoid arthritis, the expanding patient base due to demographic shifts and improved diagnostic rates heighten its utilization.

According to recent epidemiological data, the global market for treatments in this therapeutic class is projected to grow at a CAGR of approximately 6-8% over the next five years, driven by increasing incidence rates and adherence to clinical guidelines encouraging earlier intervention. The United States remains a dominant market, supported by high healthcare expenditure and robust reimbursement mechanisms.

Competitive Environment

Market competition is diversified, comprising branded pharmaceuticals, biosimilars, and generic equivalents, which influence pricing strategies. If NDC 00228-2896 operates under patent exclusivity, premiums are maintained. Conversely, the entry of biosimilars or generics pressures prices downward.

Major competitors include [list key players], each with their respective market shares, distribution channels, and pricing strategies. The quality differentiation, clinical trial data, and physician preference govern market positioning.


Pricing Dynamics and Historical Trends

Historical Price Trajectory

Over the past three years, the wholesale acquisition cost (WAC) for NDC 00228-2896 has exhibited [describe trend: stability, slight increase/decrease]. Factors driving these shifts include raw material costs, manufacturing efficiencies, regulatory costs, and payor negotiations.

In the U.S., the average list price hovers around $[insert approximate dollar amount] per unit, but actual transaction prices often differ due to rebates and discounts.

Regulatory and Reimbursement Factors

The drug’s reimbursement landscape is shaped by CMS policies, private insurers, and pharmacy benefit managers (PBMs). Changes in formulary status or inclusion in preferred drug lists can significantly alter the market price and volume.

Recent regulatory updates, such as the Inflation Reduction Act and modifications in biosimilar pathways, influence future price elasticity. Price controls or negotiation efforts, especially in public healthcare programs, may further impact pricing.


Forecasting Price Trends

Short-term Projection (Next 1–2 Years)

In the near term, prices are projected to tighten due to:

  • Increased generic/biosimilar entries: Likely causing a price decline of 10-15% as competition intensifies.
  • Regulatory pressures: Potential price negotiations and value-based pricing models originating from CMS and private payer negotiations.
  • Manufacturing costs: Slight increases due to supply chain fluctuations may minimally offset downward price pressures.

Estimated price range: $[insert] - $[insert] per unit, with an anticipated slight decline of 5-10% contingent on market entry of biosimilars.

Mid to Long-term Outlook (3–5 years)

Projections suggest:

  • Market consolidation: Larger pharmaceutical companies may leverage economies of scale, stabilizing prices.
  • Emergence of biosimilars: Expected to significantly reduce prices, potentially by 30-50% once biosimilar versions gain widespread adoption.
  • Regulatory changes: Policies favoring price transparency and negotiation could reduce list prices further.
  • Innovative therapy development: New drug entrants with superior efficacy profiles could shift demand patterns and influence pricing strategies.

Projected price range: $[insert] - $[insert], reflecting a downward adjustment driven by biosimilar adoption, with latent potential for stabilization if new patents or formulations arise.


Market Opportunities and Risks

Opportunities:

  • Expansion into emerging markets where healthcare infrastructure improves.
  • Adoption of value-based agreements that align price with clinical outcomes.
  • Development of combination therapies integrating NDC 00228-2896 to broaden usage.

Risks:

  • Entry of cost-effective biosimilars or generics.
  • Regulatory restrictions on reimbursement or pricing.
  • Supply chain disruptions impacting availability and costs.

Key Drivers Influencing Future Pricing

Drivers Impact Description
Patent expirations Negative Entry of biosimilars reduces premium pricing
Market expansion Positive Growing prevalence of target condition boosts volume
Regulatory policies Variable Price negotiations and cost-control measures can suppress prices
Innovation Mixed New formulations or combination therapies may elevate prices initially

Conclusion

NDC 00228-2896 faces a complex and evolving market landscape characterized by rising demand but increasing price competition. Short-term price stability may give way to downward pressures as biosimilars enter the market, amplified by regulatory reforms aimed at controlling drug costs. Stakeholders must monitor regulatory developments, patent statuses, and competitive moves to adapt pricing and market strategies accordingly.


Key Takeaways

  • The current pricing of NDC 00228-2896 is around $[insert], with stable demand in its primary markets.
  • The imminent entrance of biosimilars is poised to decrease prices by an estimated 30-50% over the next 3-5 years.
  • Regulatory pressures and value-based pricing models are likely to further influence future price adjustments.
  • Market expansion and innovative drug formulations offer potential revenue growth opportunities.
  • Strategic planning should include monitoring patent cliffs, regulatory shifts, and competitive dynamics to optimize pricing and market positioning.

FAQs

1. What factors most significantly influence the future price of NDC 00228-2896?
The primary factors include biosimilar competition, regulatory reimbursement policies, patent expiration dates, and market demand expansion.

2. How will biosimilar entries affect the market price?
Biosimilars typically lead to a reduction in prices by providing cost-effective alternatives, often decreasing original drug prices by 30-50%, depending on market acceptance.

3. Are there regulatory policies impacting the pricing of this drug?
Yes, policies such as CMS price negotiations, rebate reforms, and federal drug pricing initiatives significantly influence market prices.

4. What are the growth prospects for NDC 00228-2896 in emerging markets?
Expanding healthcare infrastructure and rising disease prevalence present significant opportunities, although price sensitivity and regulatory hurdles may influence growth rates.

5. How should investors or manufacturers prepare for future market changes?
They should monitor patent statuses, patent cliffs, regulatory reforms, and competitor developments to adapt pricing, production, and marketing strategies proactively.


Sources:

  1. [Epidemiological data from CDC and WHO reports]
  2. [Market reports from IQVIA and EvaluatePharma]
  3. [Regulatory updates from the FDA and CMS]
  4. [Pricing trends from SSR Health and Bloomberg Intelligence]
  5. [Industry analyses from McKinsey & Company and Deloitte]

(Note: Specific figures and source citations are illustrative; actual data should be incorporated from current market reports.)

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