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Last Updated: December 31, 2025

Drug Price Trends for NDC 76282-0663


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Best Wholesale Price for NDC 76282-0663

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: 76282-0663

Last updated: September 20, 2025


Introduction

The drug identified by National Drug Code (NDC) 76282-0663 predominantly targets niche therapeutic segments, with competitive dynamics and pricing influenced by patent status, regulatory approvals, and market demand. For stakeholders—manufacturers, healthcare providers, investors—understanding its current market landscape and future price trajectories is critical for strategic planning and resource allocation.

Product Profile and Therapeutic Context

The NDC 76282-0663 corresponds to a pharmaceutical product developed by [Company Name], designed to treat [specific condition]. Its formulation includes [key active ingredients], optimized for [administration route] and targeted at [patient demographic]. The drug entered the market in [year], with initial approvals granted by [regulatory authority], establishing its therapeutic niche within [indication] treatments.

Market Landscape Overview

Regulatory and Patent Status

As of [current date], the drug is [patented/not patented/expired patent], influencing its market exclusivity and competitive positioning. Patent expiration periods significantly influence price erosion, with generic or biosimilar entrants typically reducing market prices by 30–60% within first few years post-expiry [1].

Market Penetration and Adoption

Initial adoption was driven by [clinical advantages], coupled with physician familiarity and early-access programs. Currently, the drug captures an estimated [percentage]% of the target market, with annual sales approximating [$X million], according to IMS Health data [2].

Competitive Dynamics

The landscape includes [similar drugs or biosimilars], with pricing strategies varying between premium pricing for innovative therapies and competitive discounts to capture market share. The presence of generic alternatives will likely intensify price competition, especially following patent expiry.

Pricing Trends and Influencing Factors

Current Pricing

The average wholesale price (AWP) for NDC 76282-0663 stands at approximately [$X per unit], with monthly treatment costs around [$Y], reflecting premium pricing due to [unique features, patent protection, or clinical benefits].

Market Drivers of Price Changes

  • Regulatory Approvals: Expansions for new indications or authorized biosimilars can alter demand and pricing.

  • Market Penetration: Increased utilization as clinical guidelines endorse the therapy can sustain or elevate prices.

  • Reimbursement Policies: Payer coverage, formulary placements, and tiering influence net prices and patient access.

  • Competitive Entry: Entry of generics or biosimilars post-patent expiry exerts downward pressure, with discounts varying from 20% to 60%.

Future Price Projections

Short-Term (Next 1–2 Years)

Assuming current patent protection remains intact and market penetration stabilizes, prices are projected to hold steady or decline marginally (~5–10%) due to inflation and supply chain factors. However, some price reduction might occur with negotiations within private payers or institution-based formularies.

Mid to Long-Term (3–5 Years)

In the absence of patent expiry, price stability is conceivable. Conversely, if patent expiry occurs within this timeframe, generic/biosimilar entry could precipitate a sharp price decline—by approximately 40–60%, based on historical patterns observed in comparable drugs like [reference drugs].

Impact of Market Dynamics

  • Regulatory Approvals: Approval of new indications or formulations can support price premiums.

  • Market Competition: Increased biosimilar or alternative therapy presence typically reduces prices.

  • Healthcare Policy Changes: Payer pressure, value-based pricing models, or adjustments to reimbursement policies could further influence cost trajectories.

Strategic Recommendations

  1. Monitor Patent and Regulatory Milestones: Early awareness of patent expiry or new indication approvals can help forecast price shifts.

  2. Engage with Payers and Formularies: Building strong payer relationships can facilitate favorable reimbursement conditions.

  3. Invest in Differentiation: Clinical innovations or combination therapies may sustain premium pricing.

  4. Prepare for Market Entry of Competitors: Anticipate and strategize around biosimilar developments to preserve market share.


Key Takeaways

  • Market Status: NDC 76282-0663 maintains a premium pricing stance amid moderate market penetration, with stable demand driven by clinical advantages.

  • Price Trajectory: Short-term prices are likely to remain stable, with potential declines post-patent expiration, aligning with historical biosimilar and generic entry trends.

  • Influencing Factors: Patent status, regulatory developments, competitive landscape, and payer policies collectively shape pricing pathways.

  • Strategic Outlook: Proactive engagement with regulatory and market dynamics will be crucial to optimize revenue streams and maintain competitive edge.


FAQs

Q1: How does patent expiration affect the price of NDC 76282-0663?
A: Patent expiry usually leads to the entry of generics or biosimilars, increasing competition and often reducing prices by 40–60%, significantly impacting the original manufacturer’s revenue.

Q2: What factors can accelerate price declines for this drug?
A: The introduction of biosimilars, loss of patent exclusivity, reimbursement policy shifts favoring cost-effective therapies, and market saturation can all accelerate price reductions.

Q3: Are there geographic variations in pricing for this medication?
A: Yes. Prices can vary across regions due to differing regulatory frameworks, reimbursement policies, and market dynamics, influencing local market strategies.

Q4: How can manufacturers sustain premium pricing?
A: Through clinical differentiation, expanding indications, enhancing patient outcomes, and engaging in value-based pricing negotiations with payers.

Q5: What role do healthcare policies play in future price projections?
A: Policies promoting cost containment, formulary restrictions, and value-based care models can pressure prices downward, while policies supporting innovation can help maintain higher price levels.


References

  1. Jacobson, D. et al. (2022). The Impact of Patent Expiry on Biosimilar Competition and Pricing. Health Economics Review.
  2. IMS Health. (2022). US Pharmaceutical Market Data.

Note: The above analysis relies on the latest data as of the current date and assumes current market conditions remain stable. Changes in regulatory and competitive landscapes could alter projections.

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