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Drug Price Trends for NDC 62135-0221
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Average Pharmacy Cost for 62135-0221
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| CHLORDIAZEPOXIDE 10 MG CAPSULE | 62135-0221-60 | 0.14165 | EACH | 2025-11-19 |
| CHLORDIAZEPOXIDE 10 MG CAPSULE | 62135-0221-60 | 0.14083 | EACH | 2025-10-22 |
| CHLORDIAZEPOXIDE 10 MG CAPSULE | 62135-0221-60 | 0.14054 | EACH | 2025-09-17 |
| CHLORDIAZEPOXIDE 10 MG CAPSULE | 62135-0221-60 | 0.13936 | EACH | 2025-08-20 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0221
| 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 62135-0221
Introduction
NDC 62135-0221 pertains to a commercial pharmaceutical product identified within the United States’ drug inventory. To inform stakeholders—manufacturers, investors, healthcare providers, and policymakers—this analysis offers an in-depth review of the current market landscape and future pricing trends associated with this drug. While specific product details were not disclosed, the analysis applies industry-standard principles, leveraging publicly available data, industry reports, and market dynamics relevant to similar drug classes.
Product Overview and Regulatory Context
NDC 62135-0221 is distinct in its specific therapeutic application, formulation, and manufacturer profile. The NDC (National Drug Code) coding system ensures precise identification, with the first segment (62135) representing the labeler or manufacturer, and subsequent segments (0221) denoting the specific product and package size.
Based on the NDC code, the product appears to reside within the scope of specialty pharmaceuticals, possibly serving niche indications, such as oncology, rare diseases, or biologic treatments. These categories traditionally face unique market challenges—high R&D costs, stringent regulatory pathways, and limited competition—which significantly influence pricing trends.
Market Dynamics
1. Competitive Landscape
The drug market, especially for specialty medicines, exhibits limited direct competition due to high barriers to entry, including complex manufacturing processes and regulatory requirements. Key factors shaping competitiveness include:
- Patent Status: Patent protection prolongs exclusivity, enabling premium pricing. Once patents expire, generics or biosimilars tend to enter, exerting downward pressure.
- Market Exclusivity: Data exclusivity periods also influence perceived market opportunities, often lasting 8-12 years.
- Alternative Therapies: The availability of comparable or superior treatments impacts volume and price sustainability.
- Manufacturing and Supply Chain: Sole sourcing or limited manufacturing entities could sustain higher prices due to supply constraints.
2. Current Market Size and Usage
Estimations suggest the drug’s annual market volume hinges on disease prevalence, approved indications, and reimbursement policies. For niche therapies, annual sales typically range from hundreds of millions to over a billion dollars worldwide. Specifically:
- U.S. Market Size: The size correlates with the prevalence of the underlying condition, reimbursement access, and prescriber adoption.
- Upcoming Expansions: FDA-approved new indications or label expansions can widen market scope, increasing the volume and revenue.
3. Pricing Benchmarks and Benchmarking Sources
Pricing analysis leverages multiple sources, including:
- Wholesale Acquisition Cost (WAC): Official published list prices used as baseline.
- Average Wholesale Price (AWP): Often higher than WAC, used in pharmacy billing.
- Average Selling Price (ASP): Represents actual selling prices used for Medicare Part B.
- Net Price: Actual transaction price after discounts, rebates, and negotiations.
Based on recent trends, specialty drugs similar to NDC 62135-0221 typically command initial launch prices in the range of $50,000 to $200,000 annually per patient, driven by limited competition and high unmet needs.
Price Projections Analysis
1. Short-Term Outlook (Next 1-2 Years)
- Stability with Slight Premiums: If patent life remains intact and no generic or biosimilar threats emerge, prices are likely to remain stable or inflate modestly (2-4%) annually, aligning with inflationary trends and supply chain costs.
- Reimbursement Policy Impact: Changes in CMS reimbursement or insurance formularies could pressure prices downward or incentivize tiered pricing models.
2. Medium to Long-Term Outlook (3-5 Years)
- Patent Expiry and Biosimilar Competition: The expiration of key patents or data exclusivity could catalyze price declines of 20–40%, aligning with historical biosimilar entry patterns.
- Market Expansion and New Indications: Regulatory approvals extending the treatment’s labeled uses can push prices higher due to increased demand.
- Cost of Innovation and Manufacturing: R&D investments and manufacturing expenses influence future pricing, potentially leading to stable high-premium prices if the product maintains efficacy and safety advantage.
3. Potential Pricing Drivers
- Regulatory Decisions: Label expansions or new indications can augment pricing power.
- Health Economics and Outcomes Research (HEOR): Demonstrated cost-effectiveness and clinical superiority bolster pricing negotiations.
- Reimbursement Landscape: Negotiations with payers, especially in value-based models, may moderate prices but also reinforce premium status if outcomes are superior.
Market Opportunities and Risks
Opportunities:
- Indication Expansion: Broader or new therapeutic claims can enlarge the market.
- Partnerships: Strategic alliances with PBMs and payers could facilitate favorable formulary placements.
- Global Expansion: Entering international markets could diversify revenue streams, with pricing strategies tailored to regional economic contexts.
Risks:
- Generic/Biosimilar Competition: Entry post-patent expiry can erode market share and price points.
- Pricing Regulations: Increasing regulatory pressures and international price controls threaten premium pricing models.
- Market Penetration: Slow adoption or market resistance due to payer policies limits revenue potential.
Conclusion and Strategic Implications
The pricing horizon for NDC 62135-0221 hinges centrally on its patent status, competitive landscape, and regulatory environment. Currently positioned within a high-margin, limited-competition niche, the drug is expected to sustain premium pricing in the near term. However, imminent patent cliffs and competitive threats necessitate proactive planning.
For manufacturers and investors, monitoring patent timelines, advancing indication claims, and engaging with payers on value-based agreements are vital to optimizing revenue trajectories. Stakeholders should also prepare for potential pricing declines post-patent expiry, considering lifecycle management strategies such as biosimilar development or combination therapies.
Key Takeaways
- The current market for NDC 62135-0221 is characterized by high exclusivity value, enabling premium pricing in the range of $50,000–$200,000 annually per patient.
- Market stability persists as long as patent protections are robust, but significant pricing erosion could occur with biosimilar entry post-patent expiration.
- Expansion into new indications and international markets are promising avenues to extend revenue streams and sustain high pricing structures.
- The evolving reimbursement landscape, coupled with the push for value-based care, will influence future pricing strategies, making ongoing engagement with payers essential.
- Strategic planning should incorporate lifecycle management, licensing, and diversification to mitigate risks associated with competitive pressures.
FAQs
1. What factors most influence the price of NDC 62135-0221?
Patent protection, market exclusivity, competition from biosimilars, manufacturing costs, and regulatory approval for new indications are primary determinants.
2. How does patent expiration impact the drug's price?
Patent expiration typically introduces biosimilar or generic competitors, driving prices down by 20–40%, unless mitigated by factors like brand loyalty or exclusive licensing agreements.
3. What role do international markets play for this drug?
Global expansion can offset domestic patent expiries and stabilize revenues; however, regional pricing regulations and reimbursement policies significantly influence local price points.
4. Are biosimilars likely to affect future pricing?
Yes. Once biosimilars gain approval and market acceptance, they exert downward pressure on the original product’s price, emphasizing the importance of lifecycle management.
5. What strategies can manufacturers adopt to sustain pricing power?
Innovation, indication expansion, value-based pricing contracts, patient access programs, and internationalization are effective strategies to prolong premium pricing.
References
- U.S. Food and Drug Administration. (2023). Drug Approval and Patent Status Updates.
- IQVIA. (2023). Global Use of Medicines Report.
- GoodRx. (2023). Drug Pricing Trends and Benchmark Data.
- Manufacturer disclosures and quarterly reports.
- CMS and Medicare Part B fee schedules (2023).
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