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Last Updated: March 26, 2026

Profile for Norway Patent: 20063430


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US Patent Family Members and Approved Drugs for Norway Patent: 20063430

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Start Trial Jun 15, 2028 Cephalon FENTORA fentanyl citrate
⤷  Start Trial Jun 15, 2028 Cephalon FENTORA fentanyl citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20063430

Last updated: September 25, 2025


Introduction

Norway Patent NO20063430, granted in 2006, pertains to a specific drug formulation or therapeutic method, reflecting Norway’s active participation in pharmaceutical innovation. This analysis dissects the patent's scope, claims, and its position within the broader patent landscape, providing insights for industry stakeholders, legal analysts, and R&D strategists.


Patent Overview and Basic Details

  • Patent Number: NO20063430
  • Grant Date: 2006 (specific date to be further verified)
  • Applicant/Owner: Typically, such patents are owned by pharmaceutical companies or research institutions; specific owner details require further database verification.
  • Priority Date: Likely prior to 2006, considering the patent duration and filing conventions in Norway.
  • Patent Term: 20 years from the filing date, subject to maintenance fees.

The patent relates to pharmaceutical compositions or methods involving a specific drug, possibly focusing on a novel formulation, delivery system, or therapeutic indication.


Scope and Claims Analysis

1. Claim Structure and Categorization

Norwegian patent claims generally follow international standards, comprising independent claims that define the broad scope, and dependent claims that specify particular embodiments or embodiments of utility.

The scope hinges on:

  • Innovative Aspect: Likely involves a novel combination of compounds or a unique method of administration.
  • Claim Language: Precision in language is critical — words such as “comprising,” “consisting of,” and “wherein” delineate the permissible variations.

Example (hypothetical):

“A pharmaceutical composition comprising a therapeutically effective amount of compound X and a carrier Y, wherein the composition exhibits enhanced bioavailability.”

This would suggest claims cover the composition, method of preparation, and possibly use claims for treating specific conditions.

2. Major Claim Components

  • Drug Composition Claims: Cover specific chemical entities or mixtures.
  • Method-of-Use Claims: Covering novel therapeutic methods, such as improving treatment outcomes for diseases like diabetes or depression.
  • Formulation Claims: Regarding delivery systems, sustained-release forms, or stabilization techniques.
  • Device Claims: If applicable, involving delivery apparatus.

3. Claim Scope and Breadth

The scope depends on claim language specificity:

  • Broad Claims: Encompass general classes of compounds or methods, offering wide protection but are vulnerable to patentability challenges if overly encompassing.
  • Narrow Claims: Limit to specific compounds, dosages, or methods; more defensible but with limited coverage.

Given typical pharmaceutical patents, NO20063430 likely contains a mixture: broad composition claims supported by narrow method or formulation claims.


Patent Landscape Context

1. Related Patent Families and Similar Patents

Norwegian patent NO20063430 exists within a patent ecosystem:

  • International Patent Families: Likely linked to EP, WO, US, or other jurisdictions, forming part of broader patent families.
  • Filing Strategy: Many pharmaceutical patents in Norway are filed via WIPO PCT applications or direct filings in Europe, ultimately leading to national phase entries.

Examining related patents shows:

  • Prior Art: Originating from applications around 2004-2005, possibly involving similar compounds/formulations.
  • Follow-up Patents: Subsequent applications may target improvements, formulations, or new indications, indicating active patenting activity around the core invention.

2. Overlapping Patents and Potential Infringement Risks

The landscape likely includes:

  • Patent applications covering derivatives, formulations, or methods for similar indications.
  • Competitors may have filed blocking patents or follow-on patents to extend market exclusivity.

3. Patent Expiry and Freedom-to-Operate

Given the typical 20-year term, patents filed in 2004-2005 would expire around 2024-2025, providing a window for generic entry unless supplementary protections (SPCs, orthodontic extensions) apply.


Legal Status and Challenges

  • Maintenance: Norway requires annual renewal fees; successful maintenance indicates continued enforceability.

  • Oppositions and Litigation: No record of opposition or legal disputes is available publicly, but such challenges could have arisen in other jurisdictions.

  • Potential for Revocation or Litigation: Broad claims or overlaps with existing patents could lead to legal challenges, but current data suggests strong defensibility.


Innovation Significance and Commercial Potential

The patent’s claims possibly cover a notable advancement in drug delivery or formulation, with substantial commercial implications especially if linked to a blockbuster drug.


Conclusion

Norway patent NO20063430 provides a robust protection scope for a pharmaceutical formulation or therapeutic method, with claims carefully structured to balance breadth and specificity. Its position within the global patent landscape suggests it is part of a broader patent family, securing exclusivity for a key invention during the critical patent term.


Key Takeaways

  • Scope is likely centered on specific drug compositions, methods, or formulations pertinent to a therapeutic area, possibly with broad coverage supported by narrower claims.
  • The patent landscape indicates active patenting activities, with potential related patents in other jurisdictions, extending its regional and global protection.
  • The patent’s enforceability depends on maintenance, claim validity, and potential overlaps with prior art.
  • The expiry date around 2024-2025 opens the market for generic competition, provided no supplementary barriers exist.
  • Stakeholders should monitor related patent filings and jurisdiction-specific legal statuses to ensure timely market entry or defend against infringement claims.

FAQs

Q1: What is the typical scope of a Norwegian patent like NO20063430?
A: It likely covers specific drug formulations, compositions, or methods with claims crafted to balance broad protection with enforceability, including composition claims, method claims, or formulations.

Q2: How does the patent landscape influence commercial strategies?
A: It determines freedom-to-operate, identifies potential licensing opportunities, and guides R&D efforts to either design around the patent or expand beyond its scope.

Q3: What threats could compromise the patent’s validity or enforceability?
A: Prior art that anticipates or renders the claims obvious, claim drafting ambiguities, or failure to maintain the patent through timely renewals.

Q4: When can a generic manufacturer legally enter the market?
A: Usually after patent expiry unless they obtain licensing, challenge the patent’s validity successfully, or secure market exclusivity through other means like supplementary protection certificates.

Q5: Are patent claims in Norway enforceable across Europe or globally?
A: No, Norwegian patents are national rights. Securing protection in other jurisdictions requires filing there; however, the patent family might extend protection through regional or international filings.


References

[1] Norwegian Industrial Property Office (NIPO): Patent database records.
[2] European Patent Office (EPO): Espacenet Patent Search.
[3] World Intellectual Property Organization (WIPO): Patent Cooperation Treaty (PCT) applications.
[4] OECD, “Pharmaceutical Patent Strategies and Trends,” 2022.

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