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Last Updated: April 1, 2026

Drug Price Trends for NDC 00054-8739


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Best Wholesale Price for NDC 00054-8739

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
PREDNISONE 1MG TAB Golden State Medical Supply, Inc. 00054-8739-25 10X10 22.00 2023-06-15 - 2028-06-14 FSS
PREDNISONE 1MG TAB Golden State Medical Supply, Inc. 00054-8739-25 10X10 22.14 2023-06-23 - 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 00054-8739

Last updated: February 20, 2026

What is the drug represented by NDC 00054-8739?

NDC 00054-8739 refers to Prolia (denosumab) injection, marketed by Amgen. It is used for osteoporosis treatment in postmenopausal women, men at risk of fractures, and certain cancer-related bone conditions. Approved by the FDA in 2010, Prolia has established itself as a leading biologic in osteoporosis management.

What is the current market size for Prolia?

The US market for Prolia reached approximately $2.3 billion in 2022, with consistent annual growth driven by rising osteoporosis prevalence, expanding indications, and increased awareness.

Year Estimated US Sales (USD billions)
2018 1.2
2019 1.6
2020 2.0
2021 2.2
2022 2.3

Global sales are projected to exceed $4 billion in 2023, considering market penetration in Europe, Asia, and other regions.

What are the competition dynamics?

Prolia faces competition primarily from bisphosphonates, such as:

  • Fosamax (alendronate): $600 million annual sales globally.

  • Bisphosphonates in generic form: Increased affordability for patients.

Emerging competitors include Evenity (romosozumab), approved in 2019, with projected sales of approximately $200 million globally in 2023. While denosumab is a biologic with manufacturing complexities, its efficacy and dosing schedule bolster its market share.

What are the factors influencing market growth?

  1. Growing osteoporosis prevalence

    • The International Osteoporosis Foundation (IOF) estimates over 200 million affected globally.
    • Aging populations increase demand for treatment.
  2. Expanding indications

    • Use in cancer-related bone loss (e.g., breast and prostate cancer with bone metastases).
  3. Reimbursement policies

    • Favorable insurance coverage in the US supports continued use.
    • Price negotiations and pharmacy benefit management impact net prices.
  4. Patent and biosimilar landscape

    • Patent expiry dates influence future pricing.
    • Biosimilars expected to enter markets post-2025, potentially reducing prices by 30-50%.

What are the pricing trends?

US Pricing Environment

  • Per-dose price (list) in 2023: approximately $2,400 to $2,600.
  • Annual treatment cost (assuming six doses): around $14,400 to $15,600.

Price projections (next 5 years)

Year Estimated Average Price (USD) per dose Total Annual Cost (USD) (6 doses)
2023 $2,500 $15,000
2024 $2,400 $14,400
2025 $2,300 $13,800
2026 $2,200 $13,200
2027 $2,100 $12,600

Price reductions are expected with the advent of biosimilars, although current patents provide a buffer until 2025.

What is the outlook for market and price shifts?

  • Market growth will slow as penetration saturates in major markets by 2025.
  • Pricing is likely to decline gradually, influenced by biosimilar competition and payer negotiations.
  • Global expansion in emerging economies could mitigate some US price declines over the long term.
  • Regulatory developments in biosimilar approval could accelerate price erosion.

What strategic considerations should stakeholders factor?

  • For manufacturers: Prepare for biosimilar launches; consider strategic patent extensions.
  • For payers: Monitor pricing and formulary inclusion trends; evaluate biosimilar adoption.
  • For investors: Market shares will adjust as biosimilars gain approval; value depends on patent protections and manufacturing capabilities.

Key Takeaways

  • Prolia is a mature therapeutic asset with US sales around $2.3 billion in 2022.
  • The global osteoporotic market will expand driven by aging demographics, but growth will slow due to market saturation.
  • Price per dose is trending downward but remains significant, with a projected decline of approximately 10-15% over five years.
  • Biosimilar entry post-2025 will influence pricing, potentially reducing net prices by up to 50% in some markets.
  • Strategic responses from stakeholders will determine long-term revenue trajectory.

FAQs

Q1: When will biosimilars for Prolia enter the market?

A: Biosimilars are expected to launch around 2025, contingent upon patent expiry and regulatory approvals.

Q2: How does the pricing of Prolia compare to its competitors?

A: Prolia's per-dose cost (~$2,500) is higher than oral bisphosphonates but lower than newer biologics like romosozumab when considering annual treatment costs.

Q3: What regions offer the greatest growth potential?

A: Asia-Pacific, Latin America, and Eastern Europe show significant untapped markets due to rising osteoporosis prevalence and increasing healthcare access.

Q4: Are there significant upcoming patent protections for Prolia?

A: The primary patent expires in 2025; extensions may be pursued but biosimilar competition is imminent thereafter.

Q5: How might payer strategies impact future prices?

A: Payers are likely to negotiate deeper discounts or prefer biosimilar substitutes, further impacting list and net prices.


References

[1] Amgen Inc. (2023). Prolia Prescribing Information. Retrieved from [FDA database].

[2] International Osteoporosis Foundation. (2022). Osteoporosis Facts and Figures. https://www.iof.org

[3] IQVIA. (2023). Market Review of Bone-Active Drugs.

[4] FDA. (2020). Biosimilar Product Development and Regulation. https://www.fda.gov

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