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Last Updated: December 17, 2025

Drug Price Trends for NDC 70710-1805


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Best Wholesale Price for NDC 70710-1805

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: 70710-1805

Last updated: August 6, 2025


Introduction

The drug identified by NDC 70710-1805 has garnered considerable attention within the pharmaceutical marketplace, reflecting its therapeutic significance, patent status, and commercial potential. As an analyst specializing in drug patent landscapes and market dynamics, this report offers an in-depth evaluation of current market trends, competitive positioning, patent considerations, regulatory landscape, and forecasted pricing projections.


Product Overview and Therapeutic Indication

NDC 70710-1805 corresponds to [Insert drug name], a [describe therapeutic class; e.g., monoclonal antibody, small-molecule inhibitor] used primarily for [main indications], such as [list diseases/conditions]. The drug’s mechanism of action involves [briefly detail], offering [advantages such as improved efficacy, safety, or patient compliance].

This product entered the market in [year] and has since become a [market leader/niche product], with a growing adoption rate driven by [clinical trial results, strategic partnerships, formulary inclusion].


Market Dynamics and Competitive Landscape

Market Size and Growth Potential

Globally, the [therapeutic category] market was valued at approximately $X billion in 2022, with an anticipated CAGR of X% through 2028. The specific segment for [drug class] is projected to reach $X billion by 2028, driven by increasing prevalence of [diseases], unmet medical needs, and expanding indications.

Patient Demographics and Market Penetration

The target patient demographic is characterized by [age, ethnicity, comorbidities], with an increasing patient pool due to [e.g., demographic shifts, early diagnosis]. Market penetration is influenced by factors such as [insurance coverage, reimbursement policies, physician prescribing habits].

Competitive Landscape

Key competitors include [list major competitors], which hold [percentage] of the market share collectively. Differentiating factors for [drug name] include [unique features such as dosing convenience, minimized side effects, or patent estate]. The entry of biosimilars or generic equivalents is imminent, potentially impacting pricing and market share.


Patent Status and Intellectual Property

The patent estate for [drug name], including NDC 70710-1805, is critical in projecting pricing and market exclusivity. The primary patent [number], filed in [year], covers [key aspects: formulation, method of use, delivery system] and is expected to expire around [year]. Secondary patents and exclusivity periods, such as [orphan drug designation, data exclusivity], extend market protection until [year].

Patent challenges and legal disputes, if any, can influence market dynamics. Presently, [status of patent litigation or patent extension applications] indicates that exclusive rights are likely maintained

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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.