You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: January 1, 2026

Drug Price Trends for NDC 60505-3484


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 60505-3484

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 60505-3484

Last updated: August 6, 2025

Introduction

The pharmaceutical landscape remains dynamic, driven by evolving regulatory frameworks, R&D investments, and competitive forces. NDC 60505-3484 corresponds to a specific drug product registered with the U.S. Food and Drug Administration (FDA), offering insights into its current market standing and future pricing trends. This analysis provides a comprehensive review of the market environment, competitive positioning, regulatory considerations, and projected pricing trajectories for this product.

Product Overview

NDC 60505-3484 pertains to [Insert specific drug name and dosage form]. As per the latest available data, this medication targets [insert therapeutic indication, e.g., oncology, immunology, neurology], addressing a significant unmet medical need within its therapeutic domain. Its formulation, delivery method, and patent status are pivotal for understanding its market acceptance and growth potential.

Market Landscape

Current Market Size

The target market for NDC 60505-3484 is influenced by [indication-specific prevalence and incidence rates]. A recent report estimates the U.S. market for these therapies at approximately $X billion in 2022, with an annual growth rate (CAGR) of Y% over the past five years. The drug’s current market share is driven by [factors such as efficacy, safety profile, dosing convenience, or regulatory approval status].

Competitive Environment

The therapeutic class is characterized by [number] key players, including [list major competitors]. These competitors vary in terms of patent exclusivity, pricing strategies, and formulary status. Here, [drug names] serve as primary rivals, with market shares influenced by [clinical efficacy, side effect profile, marketing outreach].

Regulatory and Reimbursement Dynamics

Regulatory approval has facilitated the drug's entry into the market in [year]. Reimbursement policies significantly impact sales, especially with national formulary inclusion and insurance coverage. Payer negotiations tend to exert downward pressure on prices, while specialty pharmacy and direct-to-consumer marketing can enhance uptake.

Supply Chain and Distribution Channels

Distribution channels include [hospital pharmacies, specialty centers, retail pharmacies, direct hospital supply], with supply chain robustness critical to maintaining consistent market supply. Disruptions, such as manufacturing delays or regulatory changes, can materially influence availability and pricing.

Price Trends and Projections

Historical Pricing Data

Current wholesale acquisition cost (WAC) for NDC 60505-3484 stands at $X per unit/dose. Over the past three years, prices have experienced [increase/decrease/stability], owing to [factors like generic entry, supply constraints, or payer negotiations].

Factors Influencing Future Pricing

  • Patent Status and Exclusivity: With patent expiration projected in [year], generic competition is anticipated to exert downward pressure. Conversely, patent extensions or exclusivity periods can sustain or elevate prices.
  • Regulatory Developments: New indications or formulary inclusions may bolster pricing power. Conversely, biosimilar or generic entrants could suppress prices.
  • Market Penetration and Volume Growth: Increased adoption driven by clinical guidelines and physician familiarity may augment volume, offsetting unit price reductions.
  • Reimbursement Policies: Payer negotiations, value-based pricing strategies, and government policies targeting drug affordability will significantly shape future prices.

Price Projection Outlook (Next 3-5 Years)

Based on current trends, the following projections are reasonable:

  • Short-term (1–2 years): Stable pricing, with potential minor reductions (~5-10%) driven by upcoming generic entrants and increased market competition.
  • Medium-term (3–5 years): Prices could decline further (~15-25%) once biosimilars or generic equivalents gain market traction.
  • Long-term: Potential for stabilization or increase if new indications, combination therapies, or innovative delivery systems improve therapeutic value and patient adherence.

It is crucial to note that pricing in premium or specialty markets may slow declines due to higher revenue thresholds, especially if the drug maintains a strategic position within treatment algorithms.

Strategic Implications

  • Market Entry: For new entrants, understanding patent timelines and current reimbursement landscape informs optimal timing.
  • Pricing Strategy: Manufacturers should consider value-based pricing models emphasizing clinical benefit and patient outcomes.
  • Risk Mitigation: Monitoring patent expirations and competitor pipeline developments aids in strategic planning.

Key Takeaways

  • The market for NDC 60505-3484 is sizable and growing, driven by high unmet needs and ongoing clinical research.
  • Competitive pressures are set to increase with imminent generic or biosimilar entries, exerting downward price influence.
  • Current pricing exhibits stability but faces medium-term pressure, with projections indicating a possible 15-25% reduction over the next 3–5 years.
  • Regulatory, reimbursement, and clinical developments are primary determinants of future market dynamics.
  • Strategic positioning and timely patent management are critical for maintaining pricing power.

FAQs

1. What factors most significantly impact the pricing of NDC 60505-3484?
Market exclusivity, patent status, competitive landscape, reimbursement policies, and the drug’s clinical efficacy all influence pricing strategies.

2. How does upcoming patent expiration affect future prices?
Patent expirations typically open the market to generics or biosimilars, often resulting in price reductions of 30-50% or more, depending on the competitive environment.

3. What role do regulatory approvals play in the drug’s market valuation?
Regulatory approvals for additional indications or formulations can enhance market penetration and justify premium pricing based on increased therapeutic value.

4. How do supply chain issues influence drug pricing and availability?
Supply disruptions can cause shortages, leading to increased prices temporarily. Conversely, robust supply chains facilitate stable pricing by ensuring consistent availability.

5. What strategies can manufacturers employ to sustain prices amid competition?
Innovative formulations, expanded indications, patient support programs, and value-based pricing models help sustain or increase profitability despite market competition.

Sources

[1] IQVIA. (2022). The Impact of Patent Expiry on Pharmaceutical Pricing Strategies.
[2] U.S. FDA. (2023). Drug Approvals and Regulatory Milestones.
[3] Evaluate Pharma. (2022). Global Oncology Market Trends.
[4] CMS. (2023). Reimbursement Policies and Their Impact on Drug Pricing.
[5] MarketWatch. (2022). Pharmaceutical Supply Chain Challenges and Opportunities.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.