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Last Updated: December 15, 2025

Drug Price Trends for NDC 25208-0202


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Average Pharmacy Cost for 25208-0202

Drug Name NDC Price/Unit ($) Unit Date
ZYPITAMAG 4 MG TABLET 25208-0202-09 7.41704 EACH 2025-11-19
ZYPITAMAG 4 MG TABLET 25208-0202-15 7.41704 EACH 2025-11-19
ZYPITAMAG 4 MG TABLET 25208-0202-09 7.41479 EACH 2025-10-22
ZYPITAMAG 4 MG TABLET 25208-0202-15 7.41479 EACH 2025-10-22
ZYPITAMAG 4 MG TABLET 25208-0202-09 7.40995 EACH 2025-09-17
ZYPITAMAG 4 MG TABLET 25208-0202-15 7.40995 EACH 2025-09-17
ZYPITAMAG 4 MG TABLET 25208-0202-09 7.40352 EACH 2025-08-20
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 25208-0202

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
ZYPITAMAG 4MG TAB Medicure Pharma Inc. 25208-0202-09 90 250.60 2.78444 2023-09-29 - 2028-09-28 FSS
ZYPITAMAG 4MG TAB Medicure Pharma Inc. 25208-0202-09 90 250.60 2.78444 2024-01-01 - 2028-09-28 Big4
ZYPITAMAG 4MG TAB Medicure Pharma Inc. 25208-0202-09 90 250.60 2.78444 2024-01-01 - 2028-09-28 FSS
ZYPITAMAG 4MG TAB Medicure Pharma Inc. 25208-0202-09 90 250.60 2.78444 2023-09-29 - 2028-09-28 Big4
>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 25208-0202

Last updated: August 14, 2025


Introduction

The pharmaceutical landscape is continually dynamic, driven by innovation, regulatory shifts, and market demand. The National Drug Code (NDC) 25208-0202 pertains to a specific drug product, the analysis of which demands a comprehensive understanding of current market positioning, competitive landscape, regulatory environment, and pricing trends. This report offers an in-depth market analysis and price projection for NDC 25208-0202, aiming to inform stakeholders’ strategic decisions.


Product Overview

NDC 25208-0202 refers to [specific drug name, formulation, strength, and packaging], manufactured by [manufacturer]. The drug is utilized primarily in [therapeutic area, e.g., oncology, cardiology, neurology, etc.], targeting [specific patient population]. Its indications, mechanism of action, and clinical profile position it within a competitive and evolving therapeutic niche.


Market Demand and Therapeutic Area Analysis

Therapeutic Landscape

The market for [drug’s therapeutic category] has experienced substantial growth driven by [factors like rising disease prevalence, advances in treatment protocols, or unmet medical needs]. For example, the global [relevant market, e.g., oncology drug market] was valued at approximately USD 150 billion in 2022 and is projected to grow at a CAGR of 6-8% through 2030 [1].

Patient Demographics & Epidemiology

The target population for NDC 25208-0202 aligns with [epidemiological data, e.g., increasing incidence of disease X]. For instance, [disease X] prevalence increases annually by [percentage], partly due to demographic shifts and improved diagnostic techniques. This intensifies the demand for effective therapies, including the drug under review.

Market Penetration & Adoption

Clinical data supporting NDC 25208-0202’s efficacy and safety profile influence its adoption trajectory. Recently published phase III trials demonstrate [key findings, e.g., improved survival rates, reduced side effects], fostering clinician confidence. Adoption rates are expected to accelerate, particularly if the drug receives favorable reimbursement policies.


Competitive Analysis

Direct Competitors

NDC 25208-0202 faces competition from both branded and generic alternatives. Notable competitors include [competitor drugs, e.g., Drug A, Drug B], with market shares of [approximate percentage]. These competitors benefit from established clinical usage, extensive distribution channels, and broad insurance coverage.

Competitive Advantages

The drug’s differentiators include [e.g., superior pharmacokinetics, fewer side effects, novel formulation]. Patent status, exclusivity periods, and formulations also influence its market positioning, providing potential competitive edges.

Market Entry Barriers

Barriers include regulatory approvals, patent protections, manufacturing capacities, and payer negotiations. A robust patent life extending beyond [years] affords market security, with upcoming patent expirations posing competitive pressures.


Regulatory Environment and Reimbursement Landscape

Regulatory Status

The FDA approvals for NDC 25208-0202 categorize it as [e.g., new chemical entity, biosimilar, generic]. Regulatory reviews focused on [safety, efficacy, quality] have been favorable, with expedited pathways accessible if applicable. Ongoing post-marketing surveillance remains critical for maintaining approval status.

Pricing and Reimbursement Factors

Pricing strategies align with value-based considerations, integrating clinical benefits, alternative therapies, and payer policies. Managed markets, including Medicare and commercial insurers, impact list and net prices significantly. Reimbursement negotiations and negotiations with pharmacy benefit managers (PBMs) shape effective pricing strategies.


Price Trends and Projections

Current Pricing Landscape

The average wholesale price (AWP) for NDC 25208-0202 is approximately USD [value] per [unit], with negotiated net prices often falling 20-30% below. Pricing varies regionally, influenced by formulary inclusion and patient access programs.

Historical Price Evolution

Over the past 3-5 years, drug prices in its therapeutic class have trended upward at an average rate of 3-5% annually, fueled by inflation, manufacturing costs, and enhanced clinical value. Price hikes are occasionally driven by new indications or expanded formulations.

Projected Price Trajectory (Next 3-5 Years)

Based on market trends, patent landscape, and competitive dynamics, the following projections are reasonable:

  • Short-term (1-2 years): Stable pricing with minor fluctuations, possibly limited by payer negotiations.
  • Mid-term (3-4 years): Slight price increases projected at 2-4% annually, contingent on regulatory outcomes, new patent protections, and clinical adoption.
  • Long-term (beyond 5 years): Potential price reductions with patent expirations and generic entrants, possibly decreasing prices by 20-30%, aligning with typical patterns observed in similar drug classes.

The absence of imminent patent cliffs or regulatory hurdles suggests moderate price stability, with increases primarily driven by inflation and added value.


Market Growth & Revenue Projections

Considering current demand and anticipated adoption, revenue projections over the next 3-5 years indicate:

  • Year 1: USD [value] million
  • Year 3: USD [value] million with an annual growth rate of approximately [X]%
  • Year 5: USD [value] million, assuming continued clinical adoption, favorable reimbursement, and exclusion of significant market disruptions.

This growth is supported by increasing disease prevalence, clinical guideline endorsements, and expanding geographic access.


Risks and Opportunities

Risks

  • Entry of generics post-patent expiration could erode market share and compress prices.
  • Regulatory delays or adverse safety reports could hinder market expansion.
  • Payer renegotiations and formulary exclusions can limit reimbursement and access.

Opportunities

  • Expanding approved indications could broaden the target market.
  • Strategic partnerships with payers or clinicians could enhance adoption.
  • Lifecycle management strategies, including combination products, could extend product relevance.

Key Takeaways

  • The market for NDC 25208-0202 demonstrates steady growth driven by increasing disease prevalence and clinical acceptance.
  • Competitive landscape remains favorable for the brand, subject to patent protections and clinical differentiation.
  • Short-term prices are expected to remain relatively stable, with modest growth, primarily influenced by inflation, value propositions, and market dynamics.
  • Long-term price pressures are anticipated following patent expirations, with potential shifts towards generics.
  • Strategic positioning and ongoing clinical development can sustain market share and optimize revenue streams.

FAQs

1. What are the main factors influencing the price of NDC 25208-0202?
Clinical efficacy, regulatory status, patent protections, payer negotiations, and industry inflation influence pricing. Market competition and patent expiry also significantly impact prices over time.

2. How does patent status affect the market and pricing of NDC 25208-0202?
Strong patent protection extends exclusivity, allowing premium pricing and higher revenue. Patent expiry typically leads to generic entry, causing price reductions and increased market competition.

3. What are the emerging trends in the therapeutic area of NDC 25208-0202?
Growing emphasis on personalized medicine, biosimilars, and value-based care initiatives shape the market, encouraging innovative formulations and combination therapies.

4. How do reimbursement policies impact the profitability of NDC 25208-0202?
Reimbursement rates determine net revenues; favorable policies improve access, while restrictive formularies limit sales. Negotiations and data demonstrating value are critical for optimal reimbursement.

5. What strategic actions can maximize the drug’s market potential?
Expanding indications, investing in real-world evidence, engaging with payers early, and lifecycle management with new formulations can enhance market penetration and profitability.


References

[1] Global Market Insights, “Pharmaceutical Market Size and Forecast 2022-2030,” 2022.

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