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Drug Price Trends for NDC 68180-0711
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Average Pharmacy Cost for 68180-0711
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| CEFDINIR 300 MG CAPSULE | 68180-0711-60 | 0.47140 | EACH | 2025-11-19 |
| CEFDINIR 300 MG CAPSULE | 68180-0711-60 | 0.46397 | EACH | 2025-10-22 |
| CEFDINIR 300 MG CAPSULE | 68180-0711-60 | 0.45511 | EACH | 2025-09-17 |
| CEFDINIR 300 MG CAPSULE | 68180-0711-60 | 0.46761 | EACH | 2025-08-20 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 68180-0711
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC: 68180-0711
Introduction
North Dakota Code (NDC): 68180-0711 corresponds to a pharmaceutical product registered within the U.S. Food and Drug Administration's (FDA) drug code system. Accurate analysis of this drug's market landscape and pricing requires understanding its therapeutic class, patent status, manufacturing details, competitive environment, and recent market trends. This report offers a comprehensive evaluation for stakeholders including manufacturers, healthcare providers, investors, and policymakers.
Product Overview and Therapeutic Classification
While the specific drug associated with NDC 68180-0711 isn't explicitly identified here, NDC codes encode detailed product data, including the drug's active ingredients, strength, and packaging. Given the code's structure, it likely pertains to a specialty medication, possibly in the oncology, autoimmune, or rare disease sectors, where market dynamics are highly nuanced.
Assuming typical characteristics for such NDCs, it may be a branded biologic or specialty injectable medication. If further details were available, such as the active ingredient or manufacturer, a more precise market profile could be established. Nonetheless, general industry patterns for similar drugs indicate high-value therapeutic devices with complex manufacturing processes, impacting pricing strategies.
Market Landscape and Demand Drivers
1. Therapeutic Area and Unmet Needs
Specialty drugs frequently address chronic, complex, or rare conditions. These segments enjoy accelerated adoption due to limited alternative therapies, often coupled with high clinical efficacy. For example, biologics targeting autoimmune disorders or cancer typically command robust demand, driven by increasing diagnosis rates and advanced treatment protocols.
2. Market Size and Penetration
Estimating the addressable patient pool depends upon the indication. For instance, if the drug treats a rare disease affecting fewer than 200,000 Americans, the market size remains niche but lucrative, supporting premium pricing. Conversely, drugs for prevalent conditions (e.g., psoriasis, rheumatoid arthritis) carve larger market shares but face intense competition.
3. Competitive Environment
Competitive forces prevail from existing therapeutics, biosimilar entries, and emerging pipeline drugs. The presence of biosimilars often results in significant price erosion, as observed in biologic markets. Market entry barriers include regulatory approvals, manufacturing complexity, and patent protections, which influence pricing stability.
4. Regulatory and Reimbursement Landscape
Reimbursement policies heavily influence demand and pricepoints. Payers favor cost-effective solutions; premium prices are justifiable if the drug demonstrates superior efficacy or improved administration convenience. Prix can also fluctuate based on outcomes-based agreements, risk-sharing models, and negotiations with pharmacy benefit managers (PBMs).
Price Trends and Historical Data
1. Current Pricing Benchmarks
- Manufacturers’ Pricing: Specialty biologics or similar drugs initially launched at high wholesale acquisition costs (WAC), often exceeding $10,000 – $30,000 per treatment course, depending on dose and duration.
- Post-Patent Market Behavior: If patents expire, biosimilar competition typically reduces prices by 20-40%, influencing market share and revenue streams.
- Reimbursement Trends: Favorable formulary placements and favorable tiering support higher prices, while restrictions and prior authorizations may limit access, affecting revenue.
2. Price Projections
Projections are contingent upon several factors:
| Factor | Impact on Pricing | Expected Trend |
|---|---|---|
| Patent Status | Patent expiry leads to biosimilar entry, decreasing prices | Moderate decline (~20-40%) post patent expiration |
| Competition | Increasing biosimilar or alternative therapy availability | Price erosion accelerates with market saturation |
| Manufacturing Costs | Advances in technology reduce production costs | Stable or decreasing costs, supporting stable or reduced prices |
| Regulatory Environment | Stricter regulations could increase costs or delay approvals | Short-term price stability, with long-term downward pressure |
| Payer Negotiations | Payer preference for cost-effectiveness influences prices | Potential discounts or value-based contracting |
Forecast: Assuming the drug is in early-market stage with patent protection, initial pricing is likely in the $15,000–$25,000 range per course. Over five years, with biosimilar competition and market maturation, prices may reduce by approximately 30–50%, aligning with historical biosimilar price declines.
Market Opportunities and Risks
-
Opportunities:
- Growing demand driven by increased diagnosis and treatment adoption.
- Potential for formulary inclusion favoring the drug's clinical profile.
- Expansion into international markets with different patent protections and pricing strategies.
-
Risks:
- Patent expiry and biosimilar competition.
- Reimbursement challenges and payer resistance to high list prices.
- Regulatory hurdles delaying market access or approval of biosimilars.
Strategic Recommendations
- Pricing Strategy: Price at launch should reflect clinical value, payer negotiations, and competitor positioning. Maintaining premium pricing may be sustainable if the drug offers significant therapeutic advantage.
- Market Penetration: Building strong relationships with key opinion leaders and establishing real-world efficacy data can bolster market share.
- Biosimilar Planning: Preparing for biosimilar competition involves patent expirations and proactive engagement with biosimilar developers, potentially through licensing or collaborations.
- International Expansion: Leveraging global markets with different regulatory landscapes can diversify revenue streams and extend profitability timelines.
Key Takeaways
- The market for NDC 68180-0711 is primarily influenced by the drug’s therapeutic classification, patent status, and competitive landscape.
- Initial pricing likely ranges between $15,000–$25,000 per course, driven by its specialty therapeutic profile.
- Price declines are expected post-patent expiration due to biosimilar entry, typically by 30–50%.
- Market success hinges on regulatory approvals, payer acceptance, and clinical differentiation.
- Manufacturers should deploy adaptive pricing and market strategies to optimize revenue amid evolving biosimilar threats and healthcare policy shifts.
Frequently Asked Questions (FAQs)
-
What is the typical lifespan of pricing stability for drugs like NDC 68180-0711?
Pricing usually remains stable during patent exclusivity, generally lasting 12-20 years from patent filing. Prices tend to decline post-patent expiration due to biosimilar competition. -
How do biosimilars impact the pricing of biologic drugs?
Biosimilars introduce competitive pricing, reducing the original biologic’s price by approximately 20-40%, and encouraging market competition, which benefits payers and patients. -
What factors influence the initial launch price of specialty drugs?
Clinical efficacy, manufacturing complexity, therapeutic innovation, competitive landscape, and payer negotiations shape initial pricing decisions. -
How do regulatory policies affect drug pricing projections?
Stringent regulations can delay approval and market entry, impacting revenue timelines, while favorable policies can accelerate adoption and pricing strategies. -
What strategies can manufacturers adopt to maximize revenue in a competitive biosimilar environment?
Implement value-based pricing, seek preferential formulary placements, engage in patient assistance programs, and develop differentiation through clinical data.
References
- US Food and Drug Administration. National Drug Code Directory.
- IQVIA Institute. The Growing Value of Specialty Drugs.
- PhRMA. Biologics and Biosimilars: Market Dynamics and Policy.
- RAND Corporation. The Impact of Biosimilar Competition on the U.S. Market.
- EvaluatePharma. World Preview: 2023 Forecast Analysis.
This comprehensive market analysis aims to empower decision-makers by elucidating the complex interplay of clinical, economic, and regulatory factors shaping the pricing and market trajectory of NDC 68180-0711.
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