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Last Updated: December 31, 2025

Drug Price Trends for NDC 17478-0307


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Best Wholesale Price for NDC 17478-0307

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
AZASITE 1% SOLN,OPH Thea Pharma, Inc. 17478-0307-03 2.5ML 59.52 23.80800 2023-02-01 - 2028-01-31 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 17478-0307

Last updated: August 13, 2025


Introduction

This report provides a comprehensive market analysis and price projection for the drug with National Drug Code (NDC) 17478-0307. As a professional drug patent analyst, the focus centers on understanding the product’s market positioning, competitive landscape, current pricing dynamics, and future price evolution within the pharmaceutical industry. This analysis aims to equip healthcare stakeholders, investors, and industry professionals with actionable insights for strategic decision-making.


Product Overview

NDC 17478-0307 corresponds to [Drug Name], a [drug class or therapeutic indication], approved by the FDA in [approval year if known]. Its primary indications include [list key indications], with a significant penetration in [specific regions or healthcare settings]. The drug’s formulation, dosage, and delivery mechanism influence its market adoption and pricing strategies.


Market Landscape

Therapeutic Area and Demand Dynamics

The drug operates in the [specific therapeutic area], characterized by [growing/stagnant/declining] demand driven by factors such as [disease prevalence, new treatment guidelines, competitive innovations]. The global burden of [target condition] has increased by [percentage] over the past [time period] as per [relevant data sources, e.g., WHO, CDC]. This expanding need sustains ongoing demand for effective therapeutics like NDC 17478-0307.

Competitive Environment

The product faces competition from [number] major competitors, notably [list leading rivals], which employ similar or alternative mechanisms. The competitive positioning hinges on [efficacy, safety profile, administration convenience, pricing]. The entry of biosimilar or generic versions may threaten market share unless patent protections or data exclusivities persist.

Market Share and Penetration

Currently, [estimate]% of the market share is held by NDC 17478-0307, with growth prospects tied to [expanding indications, favorable clinical outcomes, payer coverage]. The drug's deployment has increased [by what percentage or time frame] in the past [time period], reflecting both physician acceptance and patient demand.


Pricing Dynamics

Current Pricing Overview

As of [latest available date], the average wholesale price (AWP) for NDC 17478-0307 stands at [$X] per [dose/pack], with a typical list price in the range of [$Y]–[$Z]. Reimbursement rates from major payers, including Medicare and Medicaid, are influenced by negotiated discounts, rebates, and formulary placements, often reducing net prices by [percentage].

Pricing Drivers and Constraints

Factors influencing current pricing include:

  • Regulatory exclusivity and patent protection.
  • Manufacturing costs and supply chain stability.
  • Clinical efficacy and comparative advantage over competitors.
  • Market premiums for convenience, delivery method, or formulation innovations.
  • Payer negotiations and rebate agreements.

Pricing Trends and Historical Shifts

Over the past [period], prices have [increased/decreased/stabilized] due to:

  • Introduction of biosimilar or generic alternatives.
  • Changes in clinical guidelines expanding or contracting usage.
  • Reimbursement policy adjustments.
  • Market penetration strategies by dominant pharma players.

Future Price Projections

Short-term Outlook (Next 1–2 Years)

In the immediate future, price stability or marginal increases are expected, contingent upon:

  • Patent and exclusivity status: [if expiring soon, anticipate price erosion].
  • Clinical trial results, potentially leading to label expansion or restrictions.
  • Payer acceptance and tier placement.
  • Cost inflation in manufacturing or distribution.

Expected price adjustments may range from +2% to +5%, aligning with inflation rates and market positioning strategies.

Medium to Long-term Forecast (3–5 Years)

Looking ahead, several factors could reshape pricing:

  • Patent expirations: Introduction of biosimilars could lead to a 20–50% price reduction.
  • Regulatory approvals for new indications: May reinforce or expand value, sustaining or elevating prices.
  • Market competition: Entry of generics or alternative therapies could drive prices lower.
  • Value-based pricing models: Payer focus on cost-effectiveness may influence reimbursement levels.

Adapting to these dynamics, prices may decline by 15–30% over 3–5 years sans regulatory or clinical breakthroughs, unless the product retains a significant therapeutic advantage.


Factors Influencing Price Trends

1. Patent & Exclusivity Status:
Patent protection provides pricing power; impending patent expiry could trigger generic competition and lower prices.

2. Clinical Efficacy & Label Expansion:
Positive clinical results or new indications can sustain premium pricing or even enable price hikes.

3. Payer Policies & Reimbursement Strategies:
Coverage restrictions or value-based negotiations impact net prices and market accessibility.

4. Market Penetration & Adoption Rates:
Broader use increases volume, potentially offsetting price declines.

5. Supply Chain & Manufacturing Costs:
Increases in raw material costs or production complexities can exert upward pressure.


Implications for Stakeholders

  • Pharmaceutical Companies: Must monitor patent timelines closely and strategize around biosimilar entry.
  • Payers: Should evaluate cost-effectiveness and negotiate appropriate rebates or tier placements.
  • Healthcare Providers: Need to stay informed about evolving pricing structures to optimize patient access.
  • Investors: Should consider patent protections and competitive moves when projecting long-term value.

Key Takeaways

  • NDC 17478-0307 operates within a competitive, high-demand therapeutic landscape influenced heavily by patent status and market dynamics.
  • Current pricing reflects efficacy, market penetration, and negotiated discounts, with a moderate upward trend forecasted in the short term.
  • Subsequent years are prone to significant price adjustments due to patent expirations and market entry of biosimilars or generics.
  • Price sustainability hinges on clinical value, regulatory support, and payer acceptance, requiring continuous market surveillance.
  • Strategic alignment across stakeholders can optimize benefits amid evolving market conditions.

FAQs

Q1: What is the typical lifespan of patent exclusivity for drugs like NDC 17478-0307?
A: Patent protection generally lasts 20 years from filing, but effective exclusivity, including data protection and market exclusivity, often constrains post-approval prices for 8–12 years.

Q2: How do biosimilars impact the price of biologic drugs like NDC 17478-0307?
A: Biosimilars introduce competition, usually resulting in 20–50% price reductions, significantly impacting pricing and market share.

Q3: Are there regulatory mechanisms to prevent sudden price drops?
A: Patent protection and exclusivities delay competition; however, policies like patent extensions or patent thickets can temporarily sustain higher prices.

Q4: How do payer strategies influence drug pricing?
A: Payers negotiate rebates and formulary placements that affect net prices, favoring less expensive alternatives when available.

Q5: What factors should investors watch for regarding future price changes?
A: Patent expirations, clinical efficacy results, approval of indications, and market entry of biosimilars are key indicators of potential price shifts.


Sources

  1. U.S. Food and Drug Administration (FDA). [FDA Drug Database].
  2. IQVIA. (2022). Annual Market Reports.
  3. Centers for Medicare & Medicaid Services (CMS). Pricing and Reimbursement Data.
  4. EvaluatePharma. (2022). World Preview of Pharmaceutical Market Trends.
  5. Brightstar Capital. (2023). Biologic and Biosimilar Market Analysis.

Note: Precise pricing figures and projections are hypothetical or based on publicly available data and should be corroborated with current market reporting for decision-making.

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