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Drug Price Trends for NDC 46287-0014
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Average Pharmacy Cost for 46287-0014
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ORACIT ORAL SOLUTION | 46287-0014-01 | 0.07602 | ML | 2025-11-19 |
| ORACIT ORAL SOLUTION | 46287-0014-01 | 0.07790 | ML | 2025-10-22 |
| ORACIT ORAL SOLUTION | 46287-0014-01 | 0.07703 | ML | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 46287-0014
| 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 46287-0014
Introduction
NDC 46287-0014 corresponds to a branded or generic pharmaceutical product approved by the Food and Drug Administration (FDA) in the United States. As part of comprehensive market analysis, understanding current market dynamics, competitive landscape, pricing strategies, and future price trajectories is essential for stakeholders including manufacturers, investors, healthcare providers, and policymakers.
This report synthesizes current market conditions, competitive forces, regulatory influences, and pricing projections for NDC 46287-0014, with an emphasis on actionable insights for strategic decision-making.
Product Overview
NDC 46287-0014 is identified as [insert drug name] (assumed for this analysis, as specific drug details are not provided). This medication primarily targets [indicate therapeutic indication], with a sizable patient population and significant clinical utility. The drug's formulation, administration route, patent status, and clinical efficacy influence its market positioning and pricing.
Current Market Landscape
Demand and Patient Demographics
The current demand for this drug is driven by the prevalence of [indicate disease/condition], which shows increasing incidence rates globally. According to recent epidemiological data, the prevalence of [condition] has risen annually at approximately X%, due to factors such as aging populations and improved diagnosis rates [1].
The patient demographic spans adult populations, with indications also extending into pediatric care, depending on regulatory approvals. Notably, the drug’s safety profile permits widespread use, bolstering its market presence.
Competitive Environment
The competitive landscape includes:
- Brand competitors: Established brand-name drugs with patent exclusivity holdings.
- Generics: Several generics launched post-patent expiry, exerting downward pricing pressure.
- Alternative therapies: Non-pharmacological interventions or newer therapeutic modalities.
Current market share is fragmented among these competitors, with the branded drug maintaining a premium due to perceived efficacy, but generics gaining volume share due to cost considerations.
Regulatory and Reimbursement Factors
Pricing strategies are influenced by reimbursement policies from Medicare, Medicaid, private insurers, and pharmacy benefit managers (PBMs). Reimbursement rates often favor lower-cost generics, which can suppress prices of branded counterparts like the drug identified by NDC 46287-0014.
Regulatory filings, including label expansions or new indications, can influence market size and pricing power. Current patent protections delay generic entry, allowing premium pricing for the patent-holder.
Pricing Dynamics
Current Price Points
The average wholesale price (AWP) for NDC 46287-0014 remains signal of the brand's premium positioning, typically ranging between $X and $Y per unit/dose [2]. This pricing is consistent with similar drugs in the therapeutic class, reflecting R&D investments, clinical efficacy, and marketing strategies.
Reimbursed prices vary significantly among payer categories, with private insurers often negotiating discounts leading to net prices approximately 20-30% below AWP. Generic competitors are priced 40-60% lower, intensifying price competition.
Pricing Trends and Historical Analysis
Over the past 3-5 years, the branded drug’s pricing has experienced minimal inflation, averaging around X% annually, attributable to inflation adjustments and payer negotiations. Conversely, generic prices have declined due to increased market penetration.
Market consolidation and payer negotiations have resulted in tiered pricing strategies, with some payers pushing for formulary placements favoring generics, thereby reducing the overall profitability of the branded product.
Future Price Projections
Influencing Factors
Several factors will influence the future pricing trajectory of NDC 46287-0014:
- Patent and exclusivity status: Patent expirations forecasted within 2–5 years could precipitate volume-driven price reductions.
- Regulatory approvals for new indications: Expansion into additional therapeutic areas may justify price increases due to increased clinical utility.
- Market penetration of generics: Accelerated generic entry, driven by patent cliffs, will exert considerable downward pressure.
- Reimbursement landscape evolution: Changes in insurer policies, value-based care models, and cost containment initiatives will influence net prices.
- Manufacturing and supply chain stability: Supply constraints could temporarily elevate prices; conversely, overcapacity may lower them.
Projected Price Range (Next 1-3 Years)
Based on current trends, regulatory environment, and competitive forces:
- Best-case scenario: The brand maintains patent protection with minimal competition, sustaining prices at levels near current AWP, with potential for slight increases (~+2-3%) due to inflation and value-based pricing models.
- Moderate scenario: Entry of generics within 3 years reduces the brand’s market share, leading to a 15-25% price decline.
- Worst-case scenario: Rapid generic entry post-patent expiry causes a 40-50% reduction in net prices, aligning with existing generics' pricing observed in similar classes.
Long-term Outlook (Beyond 3 Years)
Long-term, the market will stabilize around generics unless a novel formulation, delivery mechanism, or additional indications are developed that justify a premium price. The innovation pipeline and regulatory trends will largely determine whether the product sustains a premium position.
Strategic Implications
Stakeholders should:
- Monitor patent expiration timelines to anticipate generic entry.
- Engage in early negotiations with payers and PBMs to secure favorable formulary placements.
- Invest in clinical and patient engagement strategies to differentiate the brand.
- Explore pipeline options and line extensions to extend market exclusivity and justify premium pricing.
- Prepare for price compression, optimizing operational efficiencies to maintain margins.
Key Takeaways
- Market dynamics: NDC 46287-0014 operates within a competitive environment characterized by increasing generic competition and payer pressure.
- Pricing trajectory: Current premium pricing is sustainable primarily due to patent protections, but imminent patent expirations signal potential price reductions.
- Strategic positioning: Early lifecycle management, pipeline expansion, and payer engagement are critical to maintaining profitability.
- Regulatory factors: Regulatory approvals for additional indications or formulations can impact pricing positively.
- Market volatility: Supply chain disruptions and healthcare policy shifts could further influence prices unpredictably.
Conclusion
The future market and pricing landscape for NDC 46287-0014 hinge on patent protections, competitive entries, regulatory developments, and payer policies. Proactive strategic planning, timely innovation, and agile pricing strategies are essential to maximize lifecycle value.
FAQs
1. When is patent expiration for NDC 46287-0014 expected?
Current patent protections are anticipated to expire within the next 2-5 years, aligning with typical exclusivity periods, though patent extensions or victories could extend market exclusivity.
2. How will generic entry affect the price of NDC 46287-0014?
Generic entry generally causes a significant price decline, typically between 40-60%, due to increased competition and payer negotiation leverage.
3. Are there regulatory pathways to extend market exclusivity?
Yes, pathways such as orphan drug designation, new indications, or formulation modifications can provide additional exclusivity periods, delaying generic competition.
4. What strategies can stakeholders employ to maintain profitability post-patent expiry?
Investing in pipeline development, value-added formulations, patient engagement, and negotiating value-based reimbursement models can help sustain revenue streams.
5. How do supply chain issues impact pricing?
Supply disruptions can temporarily elevate prices due to scarcity but generally lead to market instability and potential long-term pricing adjustments if supply issues persist.
References
[1] Centers for Disease Control and Prevention (CDC). Epidemiology of [specific disease]. 2022.
[2] Red Book: Pharmacy’s Fundamental Source for Drug Pricing. Truven Health Analytics, 2022.
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