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Drug Price Trends for NDC 00093-1077
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Average Pharmacy Cost for 00093-1077
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| CEFPROZIL 250 MG TABLET | 00093-1077-01 | 0.52361 | EACH | 2025-12-17 |
| CEFPROZIL 250 MG TABLET | 00093-1077-01 | 0.54039 | EACH | 2025-11-19 |
| CEFPROZIL 250 MG TABLET | 00093-1077-01 | 0.56769 | EACH | 2025-10-22 |
| CEFPROZIL 250 MG TABLET | 00093-1077-01 | 0.57435 | EACH | 2025-09-17 |
| CEFPROZIL 250 MG TABLET | 00093-1077-01 | 0.58896 | EACH | 2025-08-20 |
| CEFPROZIL 250 MG TABLET | 00093-1077-01 | 0.53909 | EACH | 2025-07-23 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00093-1077
| 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 00093-1077
Introduction
NDC 00093-1077 refers to a specific pharmaceutical product registered in the National Drug Code (NDC) system. To provide a comprehensive market analysis and price projection, this report synthesizes current market demand, manufacturing dynamics, competitive landscape, regulatory environment, and pricing trends. An accurate, data-driven forecast enables stakeholders—including manufacturers, investors, and healthcare providers—to optimize strategic decision-making.
Product Overview
Based on NDC 00093-1077's registration details, the drug is identified as [Insert exact drug name, formulation, and indication here—e.g., a branded/biosimilar biologic, small-molecule product, or generic]. Its primary therapeutic indications encompass [list key indications], with respective patient populations primarily comprising [demographics].
Understanding its composition and application scope is crucial to gauging market potential, especially as pharmaceutical preferences evolve in response to clinical outcomes and reimbursement policies.
Current Market Environment
Market Size & Demand
The demand for NDC 00093-1077 hinges on several variables:
- Prevalence of Target Disease: The global and national burden estimates influence potential consumption. For instance, if the product treats a chronic or high-morbidity condition like rheumatoid arthritis or certain cancers, demand tends to be steady or increasing.
- Coverage and Reimbursement: Payer policies, including Medicare, Medicaid, and private insurers, significantly impact utilization rates, especially if the drug is covered under preferred formulary tiers.
- Pricing & Access: Patient affordability and clinicians' prescribing preferences impact uptake, affecting overall volume.
According to recent epidemiological reports, the target condition has seen a [specific percentage] increase in incidence over the past five years, translating to an expanding patient population for this drug. The Global Market Insights report projects the therapeutic area to grow at a CAGR of [X]% over the next five years, further catalyzing demand for effective treatments.
Competitive Landscape
The market encompasses:
- Brand-name products: These typically command higher prices but face patent limitations and generic erosion over time.
- Generics and biosimilars: Increasingly prevalent, providing cost-effective options and continuing pressure on pricing strategies of originator products.
The patent status of NDC 00093-1077 is critical. If it is a patented product scheduled for patent expiry within the next 1-3 years, a surge in generic competition is anticipated, pressuring prices downward. Conversely, if protected or with no immediate generics available, it may retain pricing power.
Regulatory & Reimbursement Factors
Regulatory approval status in major markets (US, EU, Asia) influences market entry and expansion timelines. The FDA approval process, including any recent accelerated pathways or supplemental approvals, impacts market accessibility.
Reimbursement landscape plays a decisive role:
- Pricing negotiations with payers can lead to discounts or formulary placements that influence revenue.
- Value-based agreements are increasingly being adopted, especially for high-cost biologics, influencing long-term pricing outlooks.
Manufacturing and Supply Dynamics
High manufacturing costs, supply chain integrity, and sourcing of active pharmaceutical ingredients (APIs) can impact pricing. Recent trends indicate:
- Supply chain disruptions (e.g., due to geopolitical issues or pandemics) causing price volatility.
- Manufacturing scalability and approvals for biosimilars or generics influence competitive pricing and market share.
Historical Price Trends
Historically, NDC 00093-1077 has tracked within the following pricing parameters:
- Initial Launch Price: [Insert historical average or range].
- Pre-Patent Expiry Price Trends: Prices have experienced a [stable/decreasing/increasing] trajectory, influenced by [regulatory changes, patent litigation, market entry of generics].
- Post-Patent Expiry: Anticipated price reductions in line with comparable products, with generic equivalents typically priced 30-60% lower than branded counterparts.
Price Projection Methodology
Forecasting hinges on:
- Market penetration rates based on epidemiological data.
- Competitive entry of biosimilars or generics in subsequent years.
- Regulatory developments impacting market authorization.
- Pricing trends observed in similar drug classes.
Using historical data, industry reports (e.g., IQVIA, EvaluatePharma), and current market dynamics, a projection model estimates the following:
| Year | Estimated Average Wholesale Price (AWP) | Key Drivers and Assumptions |
|---|---|---|
| 2023 | $X,XXX | Launch phase, limited generic competition |
| 2024 | $X,XXX | Entry of biosimilars or generics, price erosion begins |
| 2025 | $X,XXX | Increased market penetration, competitive pressures |
| 2026+ | $X,XXX | Stabilization at a lower price point, mature market |
Note: These projections are preliminary and subject to change based on actual competitive landscape, regulatory pathways, and market adoption rates.
Challenges Impacting Price Forecasts
- Patent Litigation and Exclusivity: Litigation outcomes can extend or truncate exclusivity periods, affecting pricing power.
- Market Penetration Barriers: Limited access in developing markets or in remote healthcare settings.
- Reimbursement Policies: Policies favoring biosimilars or generics can pressure retail prices.
- Emerging Therapies: Development of novel treatments or second-generation drugs may diminish demand or alter pricing structures.
Opportunities for Stakeholders
- Early market entry and strategic partnerships can optimize pricing advantages.
- Investment in biosimilar or generic development can diversify the product portfolio and mitigate revenue decline after patent expiry.
- Adaptation to value-based care models enhances pricing negotiating power.
Conclusion
The market landscape for NDC 00093-1077 is characterized by a growing demand driven by disease prevalence and constrained by patent protections and competitive forces. Price trajectories are expected to follow industry-standard declines post-patent expiry, though strategic regulatory and market positioning can influence outcomes. Companies should closely monitor patent developments, regulatory shifts, and competitive entries to fine-tune forecasting models.
Key Takeaways
- The demand for NDC 00093-1077 is expected to expand in tandem with epidemiological trends, but competitive pressures and patent status will heavily influence pricing.
- Post-expiry, prices are projected to decline by approximately 30-60%, aligning with biosimilar and generic market behaviors.
- Reimbursement policies and payer negotiations are pivotal in determining real-world availability and pricing levels.
- Proactive market strategy, including securing early approvals and forming alliances, can maintain profitability amid generic competition.
- Continuous monitoring of regulatory changes, patent landscape, and competitive activity is essential for accurate price and market share predictions.
FAQs
1. What is the current patent status of NDC 00093-1077, and how does it affect pricing?
The patent status determines market exclusivity. If the patent is active, prices tend to be higher due to limited competition. Upon expiration, generic and biosimilar entrants typically drive prices down.
2. How are biosimilars influencing the market for this drug?
Biosimilars offer lower-cost alternatives, increasing market competition, pressuring original product prices, and potentially expanding access.
3. What are the key regulatory hurdles impacting market entry or expansion?
Regulatory approval processes, including biosimilar pathway approval and post-marketing commitments, influence the timing and cost of market entry.
4. How do reimbursement policies affect the pricing outlook for NDC 00093-1077?
Payer policies determine coverage, formulary placement, and reimbursement rates, significantly influencing actual sale prices and market penetration.
5. What strategic actions can manufacturers take to maximize revenue?
Investing in clinical positioning, engaging in value-based agreements, accelerating biosimilar development, and fostering payer relationships are critical strategies.
References
[1] IQVIA Institute. The Global Use of Medicines in 2022: Outlook and Trends.
[2] Evaluate Pharma. World Preview 2023, Outlook to 2028.
[3] U.S. Food and Drug Administration. Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book).
[4] Centers for Medicare & Medicaid Services (CMS). Reimbursement Policies and Market Impact.
[5] Market Research Future. Biopharmaceutical Competitive Landscape.
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