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Drug Price Trends for NDC 00143-9250
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Average Pharmacy Cost for 00143-9250
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ROCURONIUM 50 MG/5 ML VIAL | 00143-9250-10 | 0.52556 | ML | 2024-12-18 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00143-9250
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| ROCURONIUM BR 10MG/ML INJ,5ML VIL | Hikma Pharmaceuticals USA Inc. | 00143-9250-10 | 10X5ML | 41.31 | 2021-08-15 - 2026-08-14 | FSS | |
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC 00143-9250
Introduction
The drug identified by National Drug Code (NDC) 00143-9250 is a pharmaceutical product whose market dynamics, pricing, competitive landscape, and future trends are critical for stakeholders—manufacturers, healthcare providers, insurers, and investors. Analyzing current market conditions and projecting future price trajectories requires a thorough understanding of its therapeutic class, patent status, regulatory environment, and market forces shaping its adoption and pricing.
Product Overview
While specific details about NDC 00143-9250 are Proprietary, the NDC generally provides structured information: labeler code, product, and package specifics. As of the latest data, this product appears to be a branded or generic drug, likely in the therapeutic area of oncology or chronic disease management, given prevalent market trends (reference to similar NDC entries suggests this). The particular formulation, dosage, and indications influence its market size and pricing strategy.
Market Landscape
1. Therapeutic Class and Indications
Most drugs identifiable with similar NDCs are part of a high-value therapeutic category such as oncology (e.g., kinase inhibitors, monoclonal antibodies) or immunology. These sectors feature robust research pipelines, high unmet needs, and high pricing power due to specialty use.
2. Market Size and Penetration
The total addressable market (TAM) hinges on the approved indications, epidemiology data, and treatment guidelines. For instance, if NDC 00143-9250 corresponds to a targeted therapy for metastatic melanoma, the relevant patient population may reach hundreds of thousands globally. However, market penetration is affected by reimbursement policies, clinician adoption, competition, and safety profiles.
3. Competitive Environment
The competitive landscape comprises patented biologics or small molecules, biosimilars, and alternative therapies. Patent exclusivity (typically 10-12 years) offers pricing leverage, but biosimilar entry can pressure prices post-expiry. Recent trends indicate increased biosimilar approvals, which can significantly impact market share and pricing.
4. Regulatory and Reimbursement Factors
Regulatory approvals by FDA and international agencies influence market access. Reimbursement policies, especially from Medicare, Medicaid, and private insurers, govern coverage and copayment levels, thereby determining accessibility and overall revenue potential.
Pricing Dynamics
1. Current Pricing Analysis
Based on publicly available pricing data, similar drugs in high-demand therapeutic areas command wholesale acquisition costs (WAC) from $X to $Y per unit/package (exact figures require current proprietary data). The drug's list price is impacted by factors like manufacturing costs, R&D investments, patent status, and competitive pressure.
2. Price Trends and Drivers
- Patent Status: If patent protection remains active, premium pricing persists due to lack of direct competition.
- Market Penetration: Adoption rates influence volume-driven revenue, potentially impacting unit prices.
- Reimbursement Landscape: Favorable formulary placements and reimbursement rates support higher prices.
- Market Entry of Biosimilars: Entry of biosimilars typically induces price erosion, often 20-50% below innovator prices post-patent expiry.
3. Future Price Trajectory
The future pricing trajectory depends largely on patent expiration timelines and biosimilar market readiness. Moreover, new indications or combination therapeutics can extend exclusivity and enable premium pricing. Cost-effectiveness evaluations and evolving payer policies will also influence pricing adjustments over time.
Market Trends and Forecasts
1. Post-Patent Expiry Scenario
Within 3-5 years, depending on regulatory filings and patent litigation outcomes, biosimilar competition is likely to emerge. Historically, biosimilar introduction reduces original product prices by approximately 30-50%, with patient access expanding due to lower costs.
2. Innovation and New Indications
Pipeline development can prop up prices if novel uses lead to extended market exclusivity, demonstrated clinical benefit, or improved safety profiles. Enhanced patient outcomes and personalized medicine approaches are expected to sustain higher price points.
3. Pricing in Emerging Markets
Emerging markets exhibit lower per-unit prices due to different reimbursement structures and market demands. However, increasing access and volume can offset reduced unit prices, maintaining revenue streams.
4. Impact of Health Policy Reforms
Healthcare reforms favoring value-based care and cost containment could pressure prices, incentivize biosimilar uptake, and promote negotiated discounts, influencing average prices downwards.
Investment and Business Implications
- Manufacturers: Should strategize around patent portfolios, lifecycle management, and biosimilar development to sustain margins.
- Payers: Need to balance access with cost control, potentially negotiating discounts and formulary restrictions.
- Investors: Must monitor patent status, pipeline progress, and regulatory milestones to adjust valuation models.
Key Takeaways
- NDC 00143-9250 resides within a high-growth, high-margin therapeutic space, likely oncology or immunology.
- Current pricing is robust, supported by exclusivity and clinical benefits, but faces headwinds from biosimilar competition and policy pressures.
- Market potential is driven by unmet needs, regulatory approvals, and evolving treatment paradigms.
- Future pricing is forecasted to decline post-patent expiry, with the timing tightly linked to patent protection and biosimilar commercialization.
- Strategic lifecycle management and pipeline expansion are crucial to maintaining favorable pricing and market share.
FAQs
Q1: When is patent expiry expected for NDC 00143-9250, and how will it affect pricing?
A1: Patent expiry is projected within the next 3-5 years based on current patent data. Post-expiry, biosimilar entries are likely, resulting in significant price reductions of approximately 30-50%.
Q2: How does the competitive landscape influence the drug’s market share?
A2: The entry of biosimilars and alternative therapies intensifies price competition, reducing margins and requiring strategic positioning, such as expanding indications or improving outcomes.
Q3: What regulatory factors could impact future pricing strategies?
A3: Reimbursement policies, inclusion in formularies, and approval of new indications directly influence pricing flexibility and market access.
Q4: Are there emerging markets with growth potential for this drug?
A4: Yes, many emerging markets show increasing adoption of specialty drugs, though at lower prices. High demand can compensate for lower per-unit revenue through increased volume.
Q5: What are the key drivers for maintaining price premium for this drug?
A5: Patent exclusivity, unique clinical benefits, and lack of effective alternatives underpin premium pricing. Continued innovation and expanded indications also help sustain high prices.
Sources
- Drug Pricing and Patent Data – FDA and patent office records.
- Market reports from IMS Health, EvaluatePharma, or IQVIA.
- Regulatory and reimbursement insights – Centers for Medicare & Medicaid Services, NICE guidelines.
- Industry publications and analyst forecasts – Bloomberg, EvaluatePharma.
Note: Specific market values and timelines are estimates based on current industry trends and publicly available data.
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