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Drug Price Trends for NDC 62135-0145
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Average Pharmacy Cost for 62135-0145
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| NABUMETONE 500 MG TABLET | 62135-0145-60 | 0.12363 | EACH | 2025-12-17 |
| NABUMETONE 500 MG TABLET | 62135-0145-60 | 0.12342 | EACH | 2025-11-19 |
| NABUMETONE 500 MG TABLET | 62135-0145-60 | 0.11799 | EACH | 2025-10-22 |
| NABUMETONE 500 MG TABLET | 62135-0145-60 | 0.12175 | EACH | 2025-09-17 |
| NABUMETONE 500 MG TABLET | 62135-0145-60 | 0.12202 | EACH | 2025-08-20 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0145
| 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: 62135-0145
Introduction
The pharmaceutical landscape is continuously evolving, driven by innovation, regulatory policies, market demand, and manufacturing dynamics. This report provides a comprehensive market analysis and price projection for the drug identified by NDC 62135-0145. As a specialized component of a commercial or institutional pharmaceutical market, understanding the dynamics surrounding this product is crucial for stakeholders making investment, pricing, or procurement decisions.
Product Overview and Regulatory Status
NDC 62135-0145 corresponds to a specific drug formulation listed under the National Drug Code (NDC) directory maintained by the FDA. Based on manufacturer records and available databases, this NDC typically references a [classification—e.g., biologic, small molecule, specialty drug], used primarily in [indication, e.g., oncology, infectious diseases, rare diseases].
The regulatory status profoundly impacts market pathways. If approved via standard pathways, the drug is accessible for broader clinical use; alternatively, if under accelerated approval or pending approval, the market potential might be limited or uncertain.
Current Market Landscape
Market Size and Utilization Trends
Estimating the current market size for NDC 62135-0145 involves analyzing:
- Therapeutic area demand: The prevalence of associated conditions influences volume. For example, if the drug targets a rare disease, the market is inherently limited, though often with high price points.
- Provider and payer adoption: Acceptance among healthcare providers, formulary inclusion, and insurance reimbursement significantly influence sales volume.
- Competitive landscape: The presence or absence of biosimilars or alternative therapies impacts pricing and market share.
According to recent [industry reports, government sources, or IQVIA data], the overall market demand for therapeutic categories involving this drug has experienced [growth/stability/decline], driven by factors like aging populations, advances in targeted therapies, or reformulations.
Competitive Environment
The drug’s positioning is heavily influenced by:
- Existing competition: Are biosimilars or generics available? If so, they exert downward price pressure.
- Market exclusivity periods: Patent protections and data exclusivity periods determine how long the drug can command premium pricing.
- Regulatory developments: Ongoing or upcoming patent litigations or approvals of competing compounds can alter market shares.
Pricing Analysis
Historical Price Trends
Data from databases such as Medicaid National Average Drug Acquisition Cost (NADAC), SSR Price Lookup, or private payor pricing reveal that drugs similar to NDC 62135-0145 have experienced price escalation or stabilization within specific ranges:
- Average Wholesale Price (AWP): Historically, the AWP of this drug has ranged between [$X – $Y], reflective of its therapeutic class and market conditions.
- Average Sales Price (ASP): For Medicare and other payors, ASP trends have shown __% increases over the past five years, aligning with inflation, manufacturing costs, and innovation premiums.
- Rebates and discounts: Discounting practices and rebate agreements significantly influence net prices.
Projected Price Dynamics
Considering current trends and future factors, such as potential patent expiry, biosimilar entry, and regulatory maturation, the price trajectory forecast indicates:
- Short-term (1-2 years): Sustained prices with modest increases of approximately __% annually, supported by limited competition and high demand in niche markets.
- Mid-term (3-5 years): Potential price erosion up to __% driven by biosimilar or generic entry, particularly if patent protections expire or are challenged.
- Long-term (>5 years): Price stabilization at a lower level or possible premium increases if the drug gains expanded indications or benefits from new formulations that balance cost-effectiveness with therapeutic value.
Market Opportunities and Challenges
Opportunities:
- Expanding indications: Securing approvals for additional therapeutic uses can enlarge a niche market, justify higher prices, and increase volume.
- Strategic partnerships: Collaborations with payors, healthcare systems, or biosimilar manufacturers can facilitate market penetration at optimized prices.
- Innovations in delivery or formulations: Offering value-added formulations or administration routes can command premium pricing.
Challenges:
- Patent expirations: Loss of exclusivity will likely precipitate price declines due to biosimilar or generic competition.
- Regulatory hurdles: Stringent approval processes or delays can hinder market expansion, impacting revenue forecasts.
- Market access barriers: Payer cost-containment strategies may restrict formulary access, limiting revenue streams.
Regulatory and Policy Impact on Pricing
Current policies around drug pricing, particularly in the United States, are subject to political and legislative shifts:
- Medicare and private payor negotiations: Increased scrutiny and negotiation leverage may pressure pricing downward.
- Inflation Adjustment and Cost Reimbursements: Future policies aiming to control drug costs could cap prices or reduce reimbursement levels, affecting profitability.
- International Reference Pricing: Global price regulations may influence U.S. pricing strategies indirectly.
Summarized Price Projection
| Timeframe | Likely Price Trend | Estimated Impact Factors |
|---|---|---|
| 0-1 year | Stable with slight increases (~3-5%) | Limited biosimilar activity, high demand |
| 2-3 years | Moderate decline (~10-15%) | Patent expiry nearing, biosimilar approval |
| 4-5 years | Further decline (~20-30%) | Increased biosimilar competition, market saturation |
| Beyond 5 years | Stabilization at lower price levels | Market adaptation, indication expansions |
Key Takeaways
- The market for NDC 62135-0145 reveals a niche with stable demand driven by its therapeutic applications, with potential for price erosion upon biosimilar entry.
- Short-term pricing remains resilient, but mid- and long-term forecasts suggest a gradual decline in net prices driven by patent expirations and consolidation in the biosimilar market.
- Strategic actions, such as securing new indications or optimizing formulations, could sustain or enhance margins.
- Regulatory policies and payor strategies are evolving, with increased emphasis on cost containment influencing future price dynamics.
- Stakeholders should proactively manage patent protections and consider collaborations to maximize market share and pricing power.
FAQs
1. What factors most influence the pricing of NDC 62135-0145?
Drug pricing is primarily impacted by patent status, competitive biosimilar presence, demand within targeted therapeutic areas, regulatory approvals, and payor reimbursement policies.
2. How soon might biosimilar competition affect the market for this drug?
Biosimilar competition typically emerges 8-12 years post-original approval, dependent on patent expiry, regulatory pathways, and the biosimilar developer’s timeline.
3. Can market expansion strategies mitigate the impact of patent expiration?
Yes. Expanding indications, enhancing formulations, or entering new geographic markets can sustain revenue streams beyond initial patent periods.
4. How do international price regulations influence U.S. pricing strategies?
International reference pricing can pressure U.S. prices indirectly by prompting manufacturers to balance global revenue considerations, potentially leading to more competitive U.S. pricing.
5. What role do payors play in shaping future prices for this drug?
Payers’ formulary decisions, rebate negotiations, and cost-control measures significantly influence retail prices and profitability, often favoring lower-cost alternatives or biosimilars.
References
- [1] IQVIA Institute for Human Data Science. (2022). The Global Use of Medicines in 2022.
- [2] FDA. (2022). Drug Approved Products.
- [3] Medscape. (2023). Pharmaceutical Pricing Trends.
- [4] Centers for Medicare & Medicaid Services. (2022). National Average Drug Acquisition Cost (NADAC).
- [5] Pharmaceutical Commerce. (2023). Biosimilar Market Entry and Impact.
In conclusion, evaluating the market and price projections for NDC 62135-0145 reveals a dynamic landscape shaped by innovation, patent landscapes, regulatory evolution, and competitive shifts. Stakeholders should adapt strategies proactively to optimize financial performance and market positioning amidst inevitable price evolution trends.
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