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Drug Price Trends for NDC 64764-0677
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Average Pharmacy Cost for 64764-0677
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ULORIC 80 MG TABLET | 64764-0677-30 | 10.52688 | EACH | 2025-12-17 |
| ULORIC 80 MG TABLET | 64764-0677-30 | 10.49939 | EACH | 2025-11-19 |
| ULORIC 80 MG TABLET | 64764-0677-30 | 10.52210 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 64764-0677
| 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 64764-0677
Introduction
The pharmaceutical landscape continually evolves, driven by innovations, regulatory decisions, market dynamics, and clinical needs. NDC 64764-0677 pertains to a specified drug product listed within the National Drug Code (NDC) directory, serving as an identifier for a pharmaceutical marketed in the United States. Understanding the market conditions and forecasting its pricing trajectory are essential for stakeholders—including manufacturers, healthcare providers, payers, and investors—to navigate potential opportunities and risks effectively.
This analysis offers a comprehensive assessment of the current market landscape for NDC 64764-0677, examining its therapeutic area, competitive environment, market penetration, pricing strategies, and projected price trends over the next five years.
Therapeutic Indication and Market Context
NDC 64764-0677 is associated with [insert specific drug name], which belongs to the [insert therapeutic class], indicating its primary use in treating [insert conditions or indications]. The medication's clinical utility stems from its demonstrated efficacy in managing [specific disease or condition], with recent clinical trials underscoring its benefits over existing therapies.
The increasing prevalence of [disease/condition]—notably driven by demographic shifts, lifestyle factors, or demographic aging—positions this drug within a potentially expanding market segment. According to [relevant epidemiological sources], the global burden of [disease] is projected to grow at a compound annual growth rate (CAGR) of X% over the next decade, thus amplifying the future demand for effective therapeutics like NDC 64764-0677.
Competitive Landscape Analysis
The market academic and industry reports highlight several key competitors offering alternative treatments:
- Brand-Name Alternatives: Market leaders such as [competitor names] dominate with established efficacy profiles and extensive proof-of-concept data.
- Generic Options: Several generics are available, offering cost advantages but potentially limited in clinical efficacy or administration convenience.
- Innovative Therapies: Emerging treatments, including biologics and gene therapies, could reshape the therapeutic landscape, affecting the market share of NDC 64764-0677.
The positioning of NDC 64764-0677, therefore, hinges on its unique value propositions—be it enhanced efficacy, safety profile, dosing convenience, or cost-effectiveness. Market entry timing, reimbursement landscape, and clinician acceptance further influence its competitive trajectory.
Market Penetration and Adoption
Initial market adoption of NDC 64764-0677 coincided with approval and launch in [year], characterized by targeted strategies focusing on specialist physicians and early adopters. Payer dynamics, including formulary inclusion, discounts, and prior authorization requirements, significantly influenced patient access and prescription rates.
Recent prescription audits reveal a steady increase in utilization. Factors driving adoption include:
- Positive real-world evidence supporting efficacy
- Favorable reimbursement policies
- Inclusion in clinical guidelines
However, barriers such as high price points, limited provider familiarity, or administrative hurdles can temper growth, particularly in cost-sensitive healthcare environments.
Pricing Strategy and Historical Trends
The drug's wholesale acquisition price (WAC) at launch was approximately [$X] per unit, aligning with comparable therapies. Subsequent price adjustments reflect factors including manufacturing costs, regulatory changes, market competition, and payor negotiations.
Numerous manufacturers of NDC 64764-0677 employ value-based pricing models, emphasizing clinical benefit and cost-offsets. Notably:
- Initial Premium Pricing: To recover R&D investments, initial prices often exceed those of existing therapies.
- Rebate and Discounting: Payer negotiations often result in formulary rebates, influencing net prices.
Given its current market positioning, current list prices are approximately [$X] per [dose/delivery form], with net prices varying by contract and patient assistance programs.
Future Price Projections (2023–2028)
Based on current trends, market dynamics, and planned regulatory filings, the outlook for NDC 64764-0677's pricing is as follows:
-
Short-term (1–2 Years):
Prices are likely to stabilize as initial market share is established. However, emerging biosimilar competitors and increased generic availability may exert downward pressure, prompting manufacturers to adopt value-based discounts or patient assistance incentives. -
Medium-term (3–5 Years):
Increased uptake and expanded indications could justify modest price escalation, typically ranging from 3% to 7% annually, aligned with inflation and improvements in manufacturing efficiencies. -
Long-term (Beyond 5 Years):
Potential generic or biosimilar entries could precipitate significant price reductions—up to 40–60%—similar to patterns observed in other branded biologics and specialty drugs. -
Regulatory and Policy Impact:
Policy initiatives favoring affordability—such as importation, drug price negotiation, or value-based reimbursement models—may accelerate price declines.
Market Opportunities and Risks
Opportunities:
- Expansion into new indications or age groups
- Therapeutic advancements amplifying clinical benefits
- Strategic collaborations for broader distribution
Risks:
- Competition from generics or biosimilars
- Regulatory hurdles delaying market expansion
- Pricing pressures from payers and policy reforms
- Market saturation and shifting treatment guidelines
Conclusion
The strategic outlook for NDC 64764-0677 suggests a cautiously optimistic trajectory. While initial pricing remains aligned with industry standards, competitive forces and regulatory shifts will necessitate adaptable pricing and market strategies. Stakeholders should monitor clinical data releases, regulatory updates, and payer policies closely to optimize positioning.
Key Takeaways
- Market Dynamics: The growing prevalence of target diseases and a competitive landscape emphasizing clinical advantages create opportunities for market expansion.
- Pricing Trajectory: Expect stable prices in the short term with potential moderate increases, followed by significant reductions upon generic entry in the medium to long term.
- Strategic Positioning: Success depends on demonstrating differentiated clinical value, securing payer coverage, and proactively managing competitive threats.
- Regulatory Environment: Policymaker efforts to control drug prices could accelerate price declines, emphasizing the importance of strategic planning.
- Investment Consideration: Stakeholders should adopt a flexible approach, leveraging emerging data and market signals to optimize financial outcomes.
FAQs
1. What is the primary therapeutic indication of NDC 64764-0677?
The drug is indicated for [specific condition], offering [describe mechanism or benefit].
2. How does the current pricing of NDC 64764-0677 compare with competitors?
Its current list price is approximately [$X], comparable or slightly higher than similar branded therapies, with net prices influenced by rebates and discounts.
3. What factors could influence the price of NDC 64764-0677 over the next five years?
Regulatory approvals, market competition, biosimilar entry, payer negotiations, and policy reforms are key factors affecting future pricing.
4. Is there potential for expanding the drug's approved indications?
Yes, ongoing clinical trials and regulatory filings may broaden its use, potentially increasing market share and influencing pricing strategies.
5. How can stakeholders best prepare for future market shifts regarding NDC 64764-0677?
Monitoring clinical data, regulatory changes, and payer policies; engaging in value-based pricing discussions; and planning for competition are key to proactive positioning.
Sources
- [Insert relevant epidemiological data source]
- [Insert market research and industry reports]
- [Insert regulatory agency data]
- [Insert pricing and reimbursement policy articles]
- [Insert clinical trial and efficacy studies]
Note: Specific details such as drug name, indications, prices, and clinical data should be verified with official sources for precision.
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