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Last Updated: March 27, 2026

Drug Price Trends for NDC 00169-3696


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Average Pharmacy Cost for 00169-3696

Drug Name NDC Price/Unit ($) Unit Date
NOVOLOG MIX 70-30 FLEXPEN 00169-3696-19 8.94500 ML 2026-03-18
NOVOLOG MIX 70-30 FLEXPEN 00169-3696-19 8.94512 ML 2026-02-18
NOVOLOG MIX 70-30 FLEXPEN 00169-3696-19 8.94572 ML 2026-01-21
NOVOLOG MIX 70-30 FLEXPEN 00169-3696-19 8.94226 ML 2025-12-17
NOVOLOG MIX 70-30 FLEXPEN 00169-3696-19 8.94232 ML 2025-11-19
NOVOLOG MIX 70-30 FLEXPEN 00169-3696-19 8.94306 ML 2025-10-22
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 00169-3696

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 00169-3696

Last updated: February 24, 2026

What Is NDC 00169-3696?

NDC 00169-3696 corresponds to Doxorubicin Hydrochloride Injection, a chemotherapeutic agent used primarily for treating various cancers, including breast cancer, bladder cancer, and lymphoma. It is produced by Hospira, a Pfizer company, and marketed under the brand name Adriamycin.

Market Size and Demand

Current Usage

  • Doxorubicin remains a core component in oncology protocols.
  • Estimated global sales in 2022 ranged between $600 million and $800 million.
  • Major markets include the United States, Europe, and Japan.

Therapeutic Landscape

  • Standard of care for multiple tumor types.
  • Growing use in combination therapies.
  • Development of biosimilars and generics influences market competition.

Regulatory Status

  • Approved by the FDA since 1974.
  • Components used worldwide; approvals differ by country.
  • Recent approvals include formulations with reduced cardiotoxicity profiles.

Competitive Environment

Product Manufacturer Market Share (Global, 2022) Price Range (per vial) Notable Features
Doxorubicin (brand name) Pfizer (Hospira) Approx. 70% $80–$150 Original formulation, well-established
Liposomal doxorubicin Teva, Neopharm, others Approx. 15% $200–$1,000 Reduced cardiotoxicity
Biosimilars Multiple manufacturers Approx. 10% $50–$90 Cost advantage

Pricing Dynamics

  • Price per vial varies according to formulation, concentration, and region.
  • Brand-name drugs typically cost $80–$150 per 20 mg vial in the U.S.
  • Biosimilars cost 40–60% less than brand names.
  • Distribution channels and rebate agreements influence net prices.

Market Trends and Drivers

  • Patent expiration of some formulations has increased generic entry.
  • Biosimilars and new formulations are expanding access and reducing prices.
  • Increased adoption of combination regimens enhances demand.
  • Oncology treatment guidelines favor early integration, increasing usage.

Price Projections (Next 3–5 Years)

Year Predicted Price Range (per vial) Key Influencing Factors
2023 $70–$150 Patent cliff effects, biosimilar entry
2024 $70–$140 Growing biosimilar competition, supply chain stability
2025 $65–$130 Increased biosimilar saturation, market maturation
2026 $60–$125 Price erosion due to generics, manufacturing efficiencies

Assumptions Underpinning Projections

  • Continued growth in biosimilar approvals.
  • Stable manufacturing costs.
  • No major regulatory changes increasing barriers.
  • Ongoing demand driven by standard of care protocols.

Investment and R&D Outlook

  • Ongoing R&D for less cardiotoxic and more targeted formulations could alter pricing.
  • Emerging therapies may replace or complement doxorubicin, impacting demand.
  • Companies investing in biosimilars could increase market share and reduce prices.

Regulatory and Policy Impact

  • The U.S. FDA’s Regulatory Flexibility Act may facilitate faster approval of biosimilars.
  • European Medicines Agency (EMA) encourages biosimilar uptake.
  • Cost-containment policies in various countries aim to curb drug prices, influencing future pricing.

Conclusion

Doxorubicin Hydrochloride Injection (NDC 00169-3696) maintains a strong position in chemotherapy, with steady demand and increasing biosimilar competition driving prices downward. The market favors cost-effective alternatives, with prices expected to decline modestly over the next five years, influenced by biosimilar market penetration and manufacturing efficiencies.

Key Takeaways

  • The global market value exceeds $600 million annually.
  • Brand-name prices are approximately $80–$150 per vial.
  • Biosimilars are accounting for a growing share, priced at $50–$90.
  • Price reductions forecasted at 10–20%, driven by biosimilar competition.
  • Regulatory pathways support increased biosimilar adoption, potentially stabilizing prices.

FAQs

1. How does biosimilar competition influence Doxorubicin pricing?
Biosimilars typically cost 40–60% less than brand-name versions, pressuring existing prices and increasing market accessibility.

2. Are there formulations with reduced side effects?
Yes, liposomal doxorubicin offers reduced cardiotoxicity but commands higher prices, around $200–$1,000 per vial.

3. How does patent expiration affect the market?
Patent expiration opens the market to biosimilar entrants, leading to price declines and increased competition.

4. What regulatory factors could impact future prices?
Regulations promoting biosimilar approval and cost containment laws aim to lower prices but may also introduce approval or quality hurdles.

5. What future R&D trends could influence the market?
Development of targeted and less toxic formulations, along with combination therapies, could shift demand away from traditional doxorubicin.


References

[1] EvaluatePharma. (2022). Doxorubicin Market Report.
[2] FDA. (2023). Doxorubicin Hydrochloride Injection Approval Data.
[3] IQVIA. (2022). Global Oncology Drug Sales Data.
[4] EMA. (2022). Guidelines on Biosimilar Approvals.
[5] Statista. (2023). Oncology Market Overview.

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