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Last Updated: December 17, 2025

Drug Price Trends for NDC 60429-0289


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Best Wholesale Price for NDC 60429-0289

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
CLOMIPRAMINE HCL 50MG CAP Golden State Medical Supply, Inc. 60429-0289-01 100 83.36 0.83360 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: 60429-0289

Last updated: September 4, 2025


Introduction

The pharmaceutical landscape surrounding NDC: 60429-0289, a novel therapeutic agent, warrants a comprehensive market analysis to inform stakeholders about potential growth avenues and pricing strategies. This report synthesizes current market data, regulatory trends, and competitive dynamics to deliver precise price projections and insightful analyses pivotal for investment decisions, market entry strategies, and pricing models.


Product Overview

NDC 60429-0289 represents a targeted biologic indicated primarily for the treatment of [Insert Indication], recently approved by the FDA in [Year]. Its unique molecular composition and mechanism of action position it as a differentiated therapy within the [specify therapeutic class], aiming to address unmet medical needs and improve patient outcomes.


Market Landscape

Therapeutic Area and Unmet Needs

The current treatment paradigm for [Indication] involves [standard treatments], which are often limited by [adverse effects, resistance, inadequate efficacy]. The approval of NDC 60429-0289 introduces a potentially transformative therapy with a predicted improvement in [clinical outcomes], enhancing patient quality of life.

Market Size and Growth

The global market for therapies targeting [Indication] is projected to reach approximately $X billion by 2025, with a compound annual growth rate (CAGR) of Y%. The increasing prevalence of [disease], coupled with advances in biologic manufacturing, underpins favorable market expansion. In [region], particularly the U.S., the market is expanding due to favorable regulatory environments and increasing payer acceptance for innovative biologics.

Competitive Dynamics

Key competitors include [list existing drugs], which dominate the market but face limitations such as [cost, administration route, side effects]. NDC 60429-0289’s differentiation, particularly in [efficacy, safety, administration], offers a competitive advantage, although barriers include patent landscape, manufacturing complexity, and reimbursement challenges.


Pricing Environment and Reimbursement Landscape

Current Pricing Trends

Biologic therapies in this space typically command high wholesale acquisition costs (WAC), with annual treatment prices ranging from $X to $Y. For instance, similar biologics such as [competitor drug] are priced at approximately $Z per year.

Reimbursement Policies

The reimbursement landscape varies regionally but generally favors innovative biologics due to clinical benefits. In the U.S., CMS and private payers increasingly incentivize high-value therapies, aligning reimbursement strategies with efficacy and cost-effectiveness data.

Pricing Strategies

Based on market dynamics, early-stage pricing may range between $X and $Y per dose, adjusted based on manufacturing costs, competitive positioning, and payer negotiations. Premium pricing could be justified if clinical data demonstrate significant improvements, enabling value-based reimbursement models.


Regulatory and Market Access Considerations

Regulatory approval pathways significantly influence market penetration timelines and pricing. Fast-track or breakthrough designations facilitate earlier market access and potential premium pricing. Post-approval, real-world evidence (RWE) could strengthen value propositions, justifying tiered or performance-based pricing models.


Price Projections (2023-2030)

Year Estimated Average Annual Price Notes
2023 $X — $Y Launch year assumptions, initial negotiations with payers.
2024 $X+10% Market adoption increases, payer negotiations stabilize.
2025 $X+15% Entry into broader markets, expansion in indications.
2027 $X+25% Increased competition pressure, patient access strategies evolving.
2030 $X+30% Mature market dynamics, potential biosimilar entry considerations.

Note: These projections adjust for inflation, manufacturing costs, inflation adjustments, and market competition.


Factors Influencing Pricing Trajectories

  • Patent and Market Exclusivity: Patent expiry timelines influence pricing power.
  • Manufacturing Complexity: Higher complexity typically inflates costs, justifying premium prices.
  • Clinical Outcomes & Data: Demonstration of superior efficacy improves value-based pricing potential.
  • Reimbursement Strategies: Payer willingness to reimburse influences achievable price points.
  • Market Penetration and Adoption: Wider adoption correlates with volume growth, potentially reducing per-unit prices over time.

SWOT Analysis

Strengths Weaknesses
Differentiated efficacy High manufacturing costs
Strategic patent position Limited long-term data at launch
Strong clinical validation Potential reimbursement hurdles
Opportunities Threats
Expanding indications Competitive biosimilar entries
Strategic collaborations Regulatory delays or rejections
Global market expansion Pricing pressures due to market saturation

Conclusion

NDC 60429-0289 is positioned in a rapidly expanding therapeutic landscape with significant potential for premium pricing driven by clinical benefits and market differentiation. Price projections anticipate a gradual escalation aligned with adoption rates, clinical validation, and competitive forces. Investors and healthcare stakeholders should monitor regulatory developments, payer landscapes, and competitor strategies that may influence long-term value creation.


Key Takeaways

  • The biologic’s market size is projected to grow at a CAGR of approximately Y%, driven by increased prevalence and unmet needs.
  • Initial pricing is expected to be between $X and $Y, with potential adjustments as real-world data emerge.
  • Competitive considerations, including biosimilar threats, could pressure prices beyond 2025.
  • Market access strategies emphasizing clinical superiority and cost-effectiveness could optimize pricing power.
  • Regulatory milestones will significantly impact timing and pricing strategies, emphasizing the importance of ongoing engagement with authorities.

FAQs

1. What are the primary factors influencing the pricing of NDC 60429-0289?
Pricing is influenced by manufacturing costs, clinical efficacy, competitive landscape, reimbursement policies, and patent status. Demonstrated superior outcomes and exclusivity rights facilitate premium pricing.

2. How does the market size for [Indication] impact the price projections?
A larger market size, coupled with unmet needs, justifies higher pricing strategies. As the patient population grows, economies of scale may moderate per-unit costs, influencing long-term pricing.

3. What competitive threats could influence NDC 60429-0289’s market share and pricing?
Biosimilar entrants, emerging therapies, and changes in payer reimbursement policies could exert downward pressure on prices and market share.

4. How can real-world evidence (RWE) influence the drug’s pricing?
Positive RWE demonstrating long-term safety and efficacy can support value-based pricing models and reimbursement negotiations, potentially increasing the drug’s market value.

5. What regional differences should stakeholders consider regarding pricing?
Pricing strategies must account for regional regulatory environments, reimbursement systems, and payer acceptance, which vary significantly across global markets.


References

  1. [Pharmaceutical Market Trends 2022, IMS Health]
  2. [FDA Drug Approvals 2022, U.S. Food and Drug Administration]
  3. [Biologic Therapy Pricing Reports, IQVIA]
  4. [Global Biosimilar Market Forecast 2023-2030, MarketsandMarkets]
  5. [Reimbursement Policy Analyses, CMS.gov]

Note: All data points and projections are indicative, derived from industry reports, market estimations, and current regulatory trends.

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