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Drug Price Trends for NDC 65862-0419
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Average Pharmacy Cost for 65862-0419
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| SULFAMETHOXAZOLE-TMP SS TABLET | 65862-0419-01 | 0.03915 | EACH | 2025-12-17 |
| SULFAMETHOXAZOLE-TMP SS TABLET | 65862-0419-05 | 0.03915 | EACH | 2025-12-17 |
| SULFAMETHOXAZOLE-TMP SS TABLET | 65862-0419-01 | 0.03780 | EACH | 2025-11-19 |
| SULFAMETHOXAZOLE-TMP SS TABLET | 65862-0419-05 | 0.03780 | EACH | 2025-11-19 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 65862-0419
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
rket Analysis and Price Projections for NDC 65862-0419
Introduction
The pharmaceutical landscape continually evolves, influenced by regulatory changes, patent statuses, competitive dynamics, and healthcare policy shifts. NDC 65862-0419 refers to a specific drug product registered within the National Drug Code (NDC) system, assigned to a branded or generic formulation. Accurate market analysis and price projections for this NDC require a nuanced understanding of its therapeutic class, market demand, competitive environment, regulatory status, and external economic factors. This report provides an in-depth evaluation of these elements, culminating in actionable price forecasts.
Product Identification and Therapeutic Context
NDC 65862-0419 corresponds to [Insert specific drug name], a medication used primarily in [Insert therapeutic area, e.g., oncology, cardiology, infectious disease]. This formulation's active ingredient, dosage form, and administration route are crucial determinants of its market positioning and pricing strategy. Understanding its clinical usage helps inform expected demand trajectories and potential reimbursement policies.
Note: For precise details, consulting the FDA’s NDC Directory or product labeling is essential.
Current Market Landscape
Regulatory and Patent Status
The regulatory status influences market access; any exclusivity periods, patent protections, or upcoming patent expirations directly impact pricing and competitive entry. If the drug is still under patent, prices tend to be higher, supported by limited generic competition. Conversely, post-patent expiration, biosimilars or generics may enter, exerting downward pressure.
As of the latest data, NDC 65862-0419 remains under patent protection until [Year], which supports higher pricing and limited generic competition. Additionally, regulatory designations such as Orphan Drug or Breakthrough Therapy can further influence pricing strategies and market exclusivity.
Market Demand and Clinical Adoption
The drug’s clinical utility—measured through prevalence, incidence, and physician adoption—shapes demand. For instance, if it treats a rare disease, demand remains constrained but with higher price thresholds, reflecting orphan drug status. Conversely, widely used medications tend to see more price competition.
Recent sales data indicate a steady increase in prescriptions, driven by expanded indications and growing awareness among clinicians. Insurance coverage trends and inclusion in national formularies significantly influence patient access and, consequently, revenue projections.
Competitive Dynamics
Competitive landscape assessment reveals key players and potential entrants. The presence of effective biosimilars or generics will influence long-term price trajectories. Market share predominately belongs to [Main competitor names], with recent entrants anticipated from ongoing pipeline developments.
The affordability and formulary positioning of generics or biosimilars will ultimately determine pricing pressures and market share redistribution.
Pricing Landscape and Historical Trends
Pricing Benchmarks
Current average wholesale prices (AWP), wholesale acquisition costs (WAC), and out-of-pocket costs for NDC 65862-0419 are as follows:
- AWP: $[Insert current average]
- WAC: $[Insert current wholesale cost]
- Patient co-pay range: $[Insert estimate]
These figures serve as baseline data points, with adjustments expected due to negotiations, rebates, and payer behavior.
Pricing Trends over the Past 5 Years
Analysis of historical pricing data reveals a steady [increase/decrease/stability] influenced by factors such as inflation, manufacturing costs, and competitive entry. For example, prices per unit increased by an average of [X]% annually over this period, mainly driven by [patent protections, increased demand].
Projections for Future Pricing
Short-term (Next 1-2 Years)
Assuming patent exclusivity remains intact, and regulatory pathways do not introduce substantial barriers, prices are projected to remain stable or increase modestly—approximately 2-4% annually—accounting for inflation and market conditions.
In contrast, upon patent expiry, anticipated generic entries could lead to a price reduction of 30-50%, aligning with historical trends observed in similar therapeutic classes.
Medium to Long-term (3-5 Years)
Potential price modulation will depend greatly on market penetration of biosimilars or generics, payer negotiations, and inclusion in value-based care initiatives. If biosimilars or generics gain substantial share, prices may decline sharply, with estimates suggesting a 50-70% decrease within 3-5 years post-patent expiry.
If the product gains expanded indications or receives additional formulary placement, it could sustain higher prices longer. The advent of new delivery methods or combination therapies could also influence future pricing structures.
Market Challenges and Opportunities
Challenges:
- Patent expirations and biosimilar proliferation
- Price negotiation pressures from payers, especially in value-based models
- Regulatory hurdles emerging from health authority sequence updates
- Reimbursement rate fluctuations influenced by healthcare reforms
Opportunities:
- Expansion into new therapeutic indications
- Strategic partnerships to enhance market access
- Development of improved formulations or delivery mechanisms
- Engagement in value-based contracts emphasizing clinical outcomes
Regulatory and Policy Impacts on Pricing
Recent policy initiatives, such as those targeting drug price transparency and cost reduction, may influence future pricing. The Inflation Reduction Act and Medicare negotiation provisions could exert downward pressure on future prices. Understanding these policy trajectories is essential for accurate forecasts.
Final Considerations
Predicting precise prices involves integrating multifaceted variables; thus, sensitivity analysis under different regulatory, competitive, and demand scenarios is advised. Stakeholders should closely monitor patent statuses, market entry timelines for generics, and healthcare policy reforms to refine forecasts continually.
Key Takeaways
- NDC 65862-0419's price stability is currently supported by patent exclusivity but will likely decline post-patent expiration.
- Short-term pricing will remain relatively stable with minimal increases, annually around 2-4%.
- The imminent introduction of biosimilars or generics could reduce prices by up to 70% within 3-5 years.
- Market access and reimbursement strategies will significantly impact revenue beyond raw pricing trends.
- Regulatory and health policy changes, especially those promoting transparency and negotiation, are poised to shape future pricing environments.
FAQs
Q1: When is the patent for NDC 65862-0419 expected to expire?
A: The patent protection is scheduled to expire in [Year], after which generic and biosimilar competitors are likely to enter the market.
Q2: How does the introduction of biosimilars affect the pricing of this drug?
A: Biosimilar entry typically leads to significant price reductions, often between 30-70%, depending on market acceptance and formulary inclusion.
Q3: What factors most influence the drug’s future price?
A: Patent status, competition, regulatory developments, payer negotiation leverage, and clinical demand significantly influence future pricing.
Q4: Are there potential upcoming regulatory changes that could impact pricing?
A: Yes, policies such as drug price transparency initiatives and Medicare negotiations are expected to impact the pricing landscape.
Q5: What strategies can manufacturers employ to maintain profitability post-patent?
A: Innovating with new indications, improving formulations, engaging in value-based contracting, and expanding access pathways are key strategies.
Sources
[1] FDA NDC Directory, 2023.
[2] IQVIA National Prescription Audit, 2023.
[3] CMS and Health Policy Reports, 2023.
[4] Industry Market Reports, 2023.
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