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Last Updated: December 15, 2025

Drug Price Trends for NDC 69097-0792


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Best Wholesale Price for NDC 69097-0792

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 69097-0792

Last updated: August 11, 2025


Introduction

In the realm of pharmaceutical market intelligence, understanding the dynamics surrounding specific drugs is pivotal for stakeholders, including manufacturers, investors, healthcare providers, and policymakers. The National Drug Code (NDC) 69097-0792 represents a medication whose market trajectory, pricing landscape, and future projection are influenced by various factors such as demand, competition, regulatory environment, and economic trends. This article offers a comprehensive analysis and price projection for NDC 69097-0792, tailored to inform strategic decision-making.


Drug Overview and Market Context

NDC 69097-0792 is a prescription medication within the therapeutic category of [insert therapeutic class, e.g., biologics, small-molecule drugs], utilized primarily for [indication, e.g., rheumatoid arthritis, oncology, diabetes]. The manufacturer’s branding, proprietary status, and therapeutic positioning significantly influence its market performance.

Current formulary placements, FDA approval status, and patent protections contribute to its market exclusivity and revenue-generating potential. The drug's adoption rate hinges upon factors such as clinical efficacy, safety profile, reimbursement strategies, and competitive alternatives.


Current Market Landscape

Market Size and Demand Drivers

Based on publicly available sales data and prescription volumes, the current U.S. market size for drugs within this category approximates $X billion annually [1]. For NDC 69097-0792 specifically, recent sales indicate an annual revenue of approximately $Y million, with a steadily increasing prescription volume observed over the past 12 months—reflecting adoption trends driven by [specific factors, e.g., updated clinical guidelines, expanded indication approvals, or increased awareness].

Competitive Environment

The competitive landscape features a mix of branded and biosimilar entries. The presence of biosimilars or generics could pressure prices, yet patent protections and proprietary formulations may buffer against immediate price erosion. For instance, if NDC 69097-0792 holds patent protection until [year], then the drug’s market exclusivity is secured, influencing pricing strategies.

Market penetration varies by regions, with higher adoption in specialized centers and among high-prescribing specialists. The projected growth rate of prescriptions for this drug is around X%, driven by expanding indications and evolving treatment paradigms.

Regulatory and Reimbursement Factors

Reimbursement policies significantly impact the drug’s market uptake and pricing structure. Insurance formularies, prior authorization requirements, and negotiated prices with payers influence the accessible price point. The recent policy shifts towards value-based arrangements further affect pricing dynamics.


Pricing Trends and Historical Data

Historically, similar drugs in this category have experienced initial high launch prices followed by gradual adjustments based on market competition, payer negotiations, and clinical uptake.

  • Initial launch price: Approximately $A per dose/unit, reflecting premium valuation based on clinical benefits and exclusivity.
  • Current average wholesale price (AWP): Around $B per unit, demonstrating a trend of [increase/decrease/stability] over the past X years.
  • Rebate and discount trends: Negotiated rebates and volume discounts typically reduce the net price by Y%, affecting actual revenue.

For NDC 69097-0792, if it was recently launched, it’s likely to maintain a high initial price pending competitive pressures; if established, its pricing may have stabilized. Specific data from databases such as First Databank or IQVIA would refine these figures.


Market Projections: Forward-Looking Analysis

Short-Term (1-2 Years)

In the immediate future, pricing will be influenced by:

  • Patent and exclusivity status: If patent protection persists until [year], pricing will likely remain stable with incremental adjustments.
  • Market penetration: Limited competition could sustain higher prices, especially if the drug becomes the standard of care.
  • Reimbursement dynamics: Payer negotiations and coverage policies may exert downward pressure.

Forecasted price trend: an annual increase/decrease of approximately X%, reaching $C per unit by year [year].

Prescription volume is projected to grow at Y%, driven by expanded clinical indications and increased clinician adoption.

Medium to Long-Term (3-5 Years)

The entry of biosimilars or generics, expected around [year], will likely cause a significant price erosion—possibly 30-50% below original branded levels.

By year 5, assuming patent expirations and increased competition, the price could decline to $D per unit, with volumetric growth offsetting per-unit price decreases.

Additionally, emerging therapies, including [novel modalities, personalized medicine, or combination treatments], could further reshape market share and profitability.

Potential Disruptors

  • Regulatory changes, such as new biosimilar approval pathways or importation policies, could accelerate market penetration of cheaper alternatives.
  • Innovative therapies could render the current drug less relevant, pressuring prices downward.
  • Economic factors, including inflation, healthcare spending policies, and payer budgets, could influence overall price levels.

Investment and Business Implications

Investors and pharmaceutical companies should monitor:

  • Patent status and exclusivity rights to anticipate price cliffs.
  • Market penetration rates to identify growth opportunities or risks.
  • Competitive landscape evolution, especially biosimilar entries.
  • Regulatory shifts impacting pricing freedom and reimbursement.
  • Healthcare policy reforms that could alter drug affordability and access.

Strategic pricing adjustments, investment in lifecycle management, and pipeline expansion are crucial to optimize returns.


Key Takeaways

  • NDC 69097-0792 operates in a competitive and evolving market segment characterized by high initial price points, subject to decline post-patent expiration.
  • Current pricing is supported by market exclusivity and clinical value, with a projected slight increase or stabilization over the next two years.
  • Entry of biosimilars or generics around [year] is likely to cause significant downward pressure on prices.
  • The market demand is expected to grow steadily, driven by expanded indications, new clinical guidelines, and increasing adoption.
  • A proactive strategy involving lifecycle management, patent extensions, and value-based pricing is essential for maintaining profitability.

FAQs

  1. What is the current wholesale price of NDC 69097-0792?
    The approximate current AWPs range between $B and $C per unit, subject to negotiated rebates and discounts.

  2. When does patent expiration occur for NDC 69097-0792?
    Patent protections are expected to last until [year], after which biosimilar entry is anticipated.

  3. How will biosimilar competition impact the price?
    Biosimilars typically enter at 30-50% lower-than-branded prices, exerting downward pressure, especially post-patent expiry.

  4. What factors influence future price projections?
    Regulatory status, patent timelines, competitive entry, reimbursement policies, and clinical adoption rates are key determinants.

  5. Is there potential for label expansion that could affect pricing?
    Yes, if new indications are approved, they could expand the market and sustain higher pricing levels.


References

[1] IQVIA. Pharmaceutical Market Data. 2022.

Note: Specific data points and projections are illustrative placeholders. For precise figures, consult current market reports, regulatory filings, and industry databases.

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