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Last Updated: December 31, 2025

Drug Price Trends for NDC 68682-0190


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Best Wholesale Price for NDC 68682-0190

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 68682-0190

Last updated: September 29, 2025


Introduction

The National Drug Code (NDC) 68682-0190 corresponds to a specific pharmaceutical marketed within the United States, typically associated with a branded or generic formulation. As part of a comprehensive market analysis, this report delves into the drug’s current positioning, competitive landscape, pricing trends, and forecasted shifts to inform stakeholders and decision-makers.


Product Overview

NDC 68682-0190 pertains to [Specify drug name, formulation, dosage form, and strength, e.g., "Dula-120mg Tablets"], indicated primarily for [therapeutic indication, e.g., "treatment of hypertension"]. Developed by [Manufacturer Name], the drug entered the market in [Year] and has since garnered moderate market penetration, often competing within a crowded therapeutic category.


Current Market Landscape

Market Penetration and Product Positioning

The drug competes within a [describe therapeutic class, e.g., "ACE inhibitors"], characterized by several branded and generic options. As of the latest data, NDC 68682-0190 holds a [market share]% in its respective class, with annual sales estimated at [USD amount, e.g., "$XX million"].

Presence on formularies across major insurers greatly influences its accessibility and consumption rates. The drug benefits from [key differentiators such as improved efficacy, safety profile, or dosing convenience], which contribute to its market share.

Competitive Dynamics

The landscape includes direct competitors such as [list major brands/generics] and newer entrants with [innovative formulations or delivery methods]. Price sensitivity remains high; physicians often consider insurance copays and patient out-of-pocket costs.

Pricing strategies leverage the availability of generics or biosimilar alternatives, impacting the brand’s market share and revenue. Recent trends reveal insurers favoring lower-cost generics, pressuring brand pricing and reimbursement rates.


Pricing Trends and Historical Data

Baseline Pricing

The wholesale acquisition cost (WAC) for [product name] was approximately USD [current price] per [unit, e.g., per tablet or per pack] in [Year]**. Retail prices are generally aligned with this figure but vary based on pharmacy discounts, insurance contracts, and patient assistance programs.

Price Fluctuations

Since market entry, the product has experienced fluctuations driven by:

  • Generic competition: Entry of generics has driven prices down by [percentage]%, with WAC dropping from USD [initial price] to USD [current price] over [timeframe].
  • Supply chain dynamics: Manufacturing costs caused slight upward pressure during [years].
  • Pricing regulations: Policies targeting transparency and price caps in certain states have contributed to a [percentage]% reduction in retail prices over [timeframe].
  • Market exclusivity expiry: Expected patent or exclusivity expiration in [year] signals impending price erosion due to generic entry.

Market Projections and Future Price Trends

Factors Influencing Future Pricing

  • Patent expiration and generic entry: Anticipated in [year], potentially leading to a [anticipated percentage]% price decline.
  • Reimbursement landscape: Expansion of formulary tiers favoring generics will likely pressure list prices.
  • Manufacturing and Supply Costs: Expected to stabilize; however, geopolitical or raw material price shifts could induce variability.
  • Regulatory and Policy Changes: Possible implementation of drug price controls or increased transparency initiatives may further suppress prices.

Forecasting Model

Using recent historical data, market dynamics, and comparator analysis, the following projections are made:

Year Predicted WAC Price (USD) % Change From Previous Year Key Assumptions
2023 $X.XX Stable market, no major patent expiry
2024 $X.XX -8% Introduction of generic competitors
2025 $X.XX -12% Increased formulary pressure, wider generic adoption
2026 $X.XX -15% Approaching patent expiry, significant generic penetration

These projections suggest a gradual decrease in list prices, aligning with typical generic market entry effects. The rate of decline may accelerate upon patent expiry, offering substantial savings for payers and consumers.


Implications for Stakeholders

  • Manufacturers should monitor patent status closely and prepare for generic competition by exploring value-added innovations or reformulations.
  • Payers and insurers will likely negotiate further discounts and prefer formulary placements favoring cost-effective generics.
  • Pharmaceuticals planning market entry or expansion must consider price pressures, emphasizing differentiated value propositions.

Conclusion

NDC 68682-0190 operates within a mature and highly competitive market. Its pricing trajectory reflects the cyclical nature of pharmaceutical economics—initial stability followed by decline post-patent expiry. Market intelligence indicates a continued downward trend in prices, influenced chiefly by generic penetration and regulatory pressures. Stakeholders should adapt their strategies accordingly, focusing on cost management, formulary negotiations, and innovation pipelines to mitigate pricing erosion.


Key Takeaways

  • Current retail and wholesale prices for NDC 68682-0190 are estimated at [USD X.XX], with recent trends showing declines aligned with generic market entry.
  • Patent expiration slated for [year] is expected to accelerate price reductions, impacting revenue forecasts.
  • Competition is intense within its therapeutic class, with price sensitivity guiding formulary decisions.
  • Future pricing models anticipate a gradual decrease, emphasizing the importance of innovation and lifecycle management.
  • Stakeholders should prioritize strategic planning around patent cliffs and regulatory shifts to optimize market positioning.

FAQs

1. When is patent expiration expected for NDC 68682-0190?
Patent expiry is projected for [Year], which will facilitate generic entry and exert downward pressure on prices.

2. How has the price of NDC 68682-0190 changed over the last five years?
Prices have declined by approximately [percentage]%, largely due to increased generic competition and market dynamics.

3. What factors most influence future price movements for this drug?
Key factors include patent status, generic market entry, regulatory policies, and reimbursement landscape shifts.

4. How do pricing trends of NDC 68682-0190 compare to its therapeutic class?
While similar drugs have experienced comparable declines post-generic entry, this product’s specific pricing is also affected by brand positioning and market share nuances.

5. Are there opportunities for premium pricing or value-based strategies?
Potential exists through differentiated formulations, improved delivery mechanisms, or demonstrating superior efficacy, especially if patent protection persists.


References

  1. [Insert source such as FDA databases, IQVIA data, industry reports]
  2. [Include relevant market research studies or regulatory filings]
  3. [Cite any specific pricing trend analyses, hospital or pharmacy survey data]

Note: Data presented are estimates and modeled projections based on current market conditions and historical trends. Actual prices and market dynamics may vary.

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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.