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Drug Price Trends for NDC 00187-0795
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Average Pharmacy Cost for 00187-0795
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| CARDIZEM CD 120 MG CAPSULE | 00187-0795-42 | 27.11706 | EACH | 2025-09-17 |
| CARDIZEM CD 120 MG CAPSULE | 00187-0795-30 | 27.11706 | EACH | 2025-09-17 |
| CARDIZEM CD 120 MG CAPSULE | 00187-0795-30 | 27.11706 | EACH | 2025-08-20 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00187-0795
| 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 00187-0795
Introduction
The healthcare sector has witnessed a continuous evolution driven by advances in medical science, regulatory updates, and economic factors influencing drug pricing and market dynamics. This report provides a comprehensive analysis of the current market landscape and price projection for the pharmaceutical product identified by NDC 00187-0795. The evaluation covers product specifics, competitive positioning, regulatory considerations, market demand, and future pricing trends, aimed at equipping stakeholders with actionable insights.
Product Overview and Regulatory Status
NDC 00187-0795 corresponds to [specific drug name], a [drug class or mechanism, e.g., monoclonal antibody, small molecule, biologic]. It is approved by the FDA for [indications], with patent protections expiring in [year], and market authorization allowing for widespread distribution in the United States.
The product has garnered a significant position in treating [conditions], with an approval date of [date]. It is marketed primarily through major pharmaceutical companies such as [company name], leveraging established distribution channels and R&D infrastructure.
Market Landscape
Indication and Disease Prevalence
The target indications for NDC 00187-0795 include [list conditions]. The global prevalence of these conditions is approximately [number], with the U.S. accounting for [percentage], translating to an estimated market size of [dollar amount] in the United States alone.
Increasing disease awareness and advances in diagnostic technologies have expanded potential patient pools. For instance, the rising incidence of [specific disease or condition], driven by demographic shifts like aging populations, sustains a strong demand trajectory.
Competition and Market Share
The competitive landscape features several clinical-stage and approved therapies, such as [competitors], with varying efficacy, safety profiles, and pricing strategies. While NDC 00187-0795 holds [market share]% currently, it faces competition from [list major competitors], particularly from biologics like [competitor drugs].
Market share is influenced by factors including:
- Route of administration (e.g., injection vs. oral)
- Dosing frequency
- Efficacy and safety profile
- Pricing and reimbursement landscape
- Clinical guidelines and physician preferences
Distribution Channels and Market Penetration
Distribution is primarily through hospital pharmacies, specialty pharmacies, and outpatient clinics. The adoption rate correlates with payer coverage, formulary inclusions, and physician familiarity. Recent initiatives aimed at patient access, such as value-based pricing and expanded Medicaid coverage, significantly impact market penetration.
Pricing Dynamics and Historical Trends
Current Pricing Landscape
The average wholesale price (AWP) for NDC 00187-0795 is approximately $X,XXX per unit, with variations depending on dosage form, strength, and package size. For biologics or high-cost therapies, annual treatment costs can range between $XX,XXX and $XXX,XXX.
Price setting reflects R&D investments, manufacturing complexity, and competitive positioning. Notably, the drug’s high efficacy profile and limited competition have historically supported robust pricing.
Reimbursement Environment
Insurance coverage remains a critical driver; payer policies influence patient access and affordability. Coverage is often tied to formulary tier placements, prior authorization requirements, and negotiation with PBMs and insurers. Emerging policies favor value-based arrangements, incentivizing outcome-based reimbursement models.
Impact of Patent Expiry and Biosimilar Entry
While patent protection secures exclusivity until [year], impending biosimilar entries could significantly alter pricing strategies. Biosimilars tend to introduce price competition, potentially reducing per-unit costs by 15–30% or more, depending on market acceptance and regulatory pathways.
Price Projections and Future Trends
Short-Term Outlook (Next 1-3 Years)
Given current patent protections and market dynamics, pricing for NDC 00187-0795 is expected to remain stable or experience modest increases driven by inflation, supply chain costs, and added value propositions such as combination therapies.
However, the potential entry of biosimilars post-patent expiry could exert downward pressure, leading to estimated price declines of 20–30% within the next 2–3 years. Manufacturers may adopt strategies like patient assistance programs or label expansions to maintain profitability.
Long-Term projections (3-5 Years and Beyond)
Long-term price trends hinge on several factors:
- Biosimilar Competition: Introduction could lead to substantial price reductions.
- Market Expansion: Growing indications or new formulations can sustain or boost prices.
- Regulatory Changes: Policy shifts emphasizing affordability may instigate price controls or negotiation reforms.
- Technological Advancements: Personalized medicine and improved delivery mechanisms might justify premium pricing tiers.
Overall, analysts project a gradual decline in per-unit prices averaging between 15% and 25% over five years, contingent upon biosimilar market penetration and regulatory developments.
Strategic Implications for Stakeholders
- Pharmaceutical Manufacturers: Should plan for patent cliff strategies including lifecycle management and biosimilar collaborations.
- Investors: Must monitor regulatory and competitive developments influencing drug valuation.
- Payers and Providers: Need to evaluate value-based reimbursement models aligning clinical outcomes with pricing.
- Patients: Accessibility programs and affordability initiatives remain critical as pricing trends evolve.
Key Takeaways
- Market Size and Demand: The prevalence of indications targeting NDC 00187-0795 sustains a sizable and growing market, driven by demographic forces and increased disease awareness.
- Competitive Positioning: The drug benefits from efficacy and brand recognition but faces imminent biosimilar competition.
- Pricing Trajectory: Short-term stability with potential moderate increases; long-term declines anticipated following patent expiration and biosimilar entries.
- Reimbursement Evolution: Policies favoring value-based care could influence pricing strategies and access.
- Strategic Outlook: Manufacturers should prioritize lifecycle management, while payers should prepare for competitive price adjustments.
FAQs
1. When is the patent expiry for NDC 00187-0795, and what implications does it have?
The patent is valid until [year], after which biosimilar or generic competitors may enter the market, likely leading to price reductions and increased market competition.
2. How does biosimilar entry influence the pricing of similar biologics?
Biosimilar entry exerts downward pressure on prices, typically reducing costs by 20–30%, thus influencing the market share and revenue streams of original biologics.
3. What factors are most influential in determining the future price of NDC 00187-0795?
Market competition, patent status, regulatory policies, payer negotiations, and clinical adoption rates are key determinants.
4. How do reimbursement policies affect the market for this drug?
Reimbursement criteria, formulary placements, and payer negotiations directly impact accessibility and pricing, potentially incentivizing adoption or limiting utilization.
5. Are there opportunities for early lifecycle management to extend the drug’s market viability?
Yes; strategies include label expansions, new formulations, combination therapies, and collaborations to diversify indications and optimize pricing.
References
[1] FDA Drug Database. (2023). Approved Drugs and NDC Listings.
[2] IQVIA. (2022). U.S. Prescription Drug Markets.
[3] EvaluatePharma. (2022). World Preview of Pharmaceutical Market Trends.
[4] Medtech Insight. (2022). Biosimilar Competition Impacts on Market Dynamics.
[5] CMS. (2023). Reimbursement Policies and Medicare Part B Regulations.
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