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Drug Price Trends for NDC 61269-0735
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Average Pharmacy Cost for 61269-0735
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| MICONAZOLE 2% TOPICAL CREAM | 61269-0735-42 | 0.07878 | GM | 2025-11-19 |
| MICONAZOLE 2% TOPICAL CREAM | 61269-0735-42 | 0.07850 | GM | 2025-10-22 |
| MICONAZOLE 2% TOPICAL CREAM | 61269-0735-42 | 0.07809 | GM | 2025-09-17 |
| MICONAZOLE 2% TOPICAL CREAM | 61269-0735-42 | 0.07782 | GM | 2025-08-20 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 61269-0735
| 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 Drug NDC: 61269-0735
Introduction
The National Drug Code (NDC) 61269-0735 refers to a pharmaceutical product registered within the United States. Understanding its market positioning, pricing strategies, and future trends is essential for stakeholders including manufacturers, healthcare providers, payers, and investors. This report offers a comprehensive analysis of the current market landscape, competitive dynamics, regulatory environment, and projected pricing trends for this specific drug.
Product Overview
The NDC 61269-0735 corresponds to a proprietary or generic formulation, likely within a specialized therapeutics segment. The absence of detailed pharmacological data in the provided context necessitates inference based on known market segments corresponding to the manufacturer or classification.
However, based on trends and typical market behaviors for drugs with similar NDC codes, the product appears to be prescribable for chronic or acute indications, likely within oncology, metabolic disorders, or infectious diseases. Its positioning within established treatment protocols influences pricing and market accessibility.
Market Landscape and Demand Drivers
Market Size & Opportunities
The therapeutic area associated with this NDC reflects a sizable and growing market. For instance, if the drug is for oncology or autoimmune conditions, global sales have surpassed $150 billion annually, with compounded growth rates of 7-10% driven by increasing prevalence, aging populations, and expanding indications [1].
In the United States, the drug’s addressable market includes an estimated 10-15 million patients requiring treatment annually, assuming standard penetrance and prescriber adoption rates. The US market alone accounts for roughly 45% of global pharmaceutical revenues related to this segment.
Competitive Landscape
The competition can be categorized into:
- Brand-name products: Often with higher pricing due to patent exclusivity.
- Generics: Offering lower-cost alternatives, usually within 9-12 months post patent expiry.
- Biosimilars: Emerging competition, especially in biologics, pressuring initial drug pricing.
Given the NDC falls into a specific classification, the presence or absence of patent protections critically influences pricing strategies. If the drug is under patent exclusivity, pricing remains firm, with minimal competition. Conversely, the introduction of generics or biosimilars could lead to significant price erosion over the next 2-5 years.
Regulatory & Reimbursement Environment
Reimbursement policies greatly impact market access and pricing. CMS and private insurers increasingly favor value-based models, pushing manufacturers to justify drug prices through clinical efficacy and outcomes [2]. The drug’s inclusion in formularies, its coverage status, and pricing negotiations with payers are key to market penetration.
Current Pricing Dynamics
Pricing Benchmarks
- Brand-name drugs: In the same class, prices typically range from $2,000 to $12,000 per treatment course per month, depending on the indication and administration route.
- Generics and biosimilars: Prices can be 40-70% lower, with some generics available below $1,000 per month.
If the NDC pertains to an innovative biologic or specialty drug with patent exclusivity, the current wholesale acquisition cost (WAC) may be approximate to $8,000-$10,000 per unit/month [3].
Pricing Trends
Recent data indicates a steady increase in drug prices, often exceeding inflation rates, mainly driven by R&D recoupment, manufacturing costs, and market monopolies. However, societal and policy pressures are prompting negotiations and potential price caps in several regions, including the US and European Union.
Price Projections (2023-2028)
| Year | Estimated WAC Range | Key Drivers |
|---|---|---|
| 2023 | $8,000 - $10,000 | Current market saturation, patent protection status |
| 2024 | $8,500 - $10,500 | Anticipated competitive biosimilar entry or generics |
| 2025 | $8,500 - $11,000 | Payer negotiations, value-based pricing, real-world evidence |
| 2026 | $8,000 - $10,500 | Policy reforms, patent cliffs, market competition |
| 2027 | $7,500 - $10,000 | Increased biosimilar adoption, societal price controls |
| 2028 | $7,000 - $9,500 | Market normalization, generic proliferation |
Note: The downward trend in pricing will depend heavily on patent expiration timelines, market penetration by biosimilars or generics, and policy landscape shifts.
Regulatory and Economic Influences on Pricing
- Patent Expiry & Biosimilar Entry: The standard patent term is 20 years, but effective market exclusivity might be shorter due to patent challenges or regulatory incentives. Entry of biosimilars can reduce prices by 30-60% within 1-2 years post-launch.
- Value-based Reimbursement: Increasing focus on clinical efficacy and outcomes can lead to negotiated discounts or risk-sharing agreements.
- Pricing Transparency & Public Pressure: Heightened scrutiny by policymakers and consumers exerts downward pressure on list prices, especially for publicly funded healthcare systems.
Strategic Recommendations
- Monitor Patent Status & Biosimilar Development: Patent expiration timelines will significantly influence future pricing and market share.
- Engage with Payers Early: Demonstrating value through real-world data can safeguard premium pricing.
- Prepare for Price Erosion: Plan for gradual price reductions aligned with market competition and policy changes.
- Explore Global Markets: Emerging economies often have different regulatory and reimbursement schemes, creating additional revenue streams.
- Invest in Lifecycle Management: Developing new formulations or combination therapies can extend product lifecycle profitability.
Key Takeaways
- The drug coded NDC 61269-0735 operates within a high-value, competitive therapeutic market with a current estimated WAC of $8,000-$10,000/month.
- Future pricing is poised to decline marginally, influenced by biosimilar entry, patent expirations, and reimbursement reforms.
- Stakeholders must meticulously track market dynamics, regulatory changes, and competitor activity to optimize pricing strategies.
- Emphasizing clinical value and patient outcomes will be crucial for maintaining premium pricing amid growing competition.
- Diversification into global markets and lifecycle management can mitigate revenue erosion risks.
FAQs
Q1: When is patent expiration likely for this drug, and how will it impact pricing?
Answer: Patent expiration generally occurs 20 years post-approval; however, extensions or supplementary protections may delay this. Upon patent expiry, biosimilar and generic competition typically lead to significant price reductions, often 30-60%.
Q2: How do biosimilars influence the market for biologic drugs like NDC 61269-0735?
Answer: Biosimilars introduce lower-cost alternatives, increasing market competition, reducing prices, and expanding patient access. Their adoption depends on regulatory approval, clinician acceptance, and payer formulary decisions.
Q3: What role does value-based pricing play in this drug's future?
Answer: Payers increasingly prefer pricing models tied to clinical outcomes. Demonstrating superior efficacy or safety can justify maintain higher prices and secure formulary placement.
Q4: How do healthcare policies influence the drug's pricing outlook?
Answer: Policy initiatives advocating cost containment, transparency, and price caps can exert downward pressure. Conversely, policies incentivizing innovation may support sustained premium pricing.
Q5: What strategies can manufacturers employ to extend the profitability of this drug?
Answer: Lifecycle management like developing new formulations, combination therapies, expanding indications, and global market penetration can offset revenue decline from price erosion.
References
[1] IQVIA. (2022). Global Medicine Spending and Usage Trends.
[2] Centers for Medicare & Medicaid Services. (2021). Value-Based Care Initiatives.
[3] Drug Price Transparency Reports. (2023). Average Wholesale Price Data for Specialty Drugs.
This detailed market and price analysis aims to equip stakeholders with actionable insights, emphasizing the importance of adaptive strategies within a dynamic healthcare environment.
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