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Drug Price Trends for NDC 62135-0495
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Average Pharmacy Cost for 62135-0495
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| GRISEOFULVIN ULTRA 250 MG TAB | 62135-0495-01 | 3.83976 | EACH | 2025-11-19 |
| GRISEOFULVIN ULTRA 250 MG TAB | 62135-0495-30 | 3.83976 | EACH | 2025-11-19 |
| GRISEOFULVIN ULTRA 250 MG TAB | 62135-0495-01 | 4.05580 | EACH | 2025-10-22 |
| GRISEOFULVIN ULTRA 250 MG TAB | 62135-0495-30 | 4.05580 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0495
| 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: 62135-0495
Introduction
NDC: 62135-0495 refers to a specific pharmaceutical product registered with the National Drug Code (NDC) system managed by the U.S. Food and Drug Administration (FDA). To evaluate its market landscape and forecast pricing trends, it is essential to understand its therapeutic indication, manufacturing details, competitive environment, market demands, and reimbursement landscape. This analysis synthesizes recent market data, industry trends, and regulatory developments to offer a comprehensive outlook for stakeholders.
Product Overview
The NDC 62135-0495 identifies [Insert specific drug name, formulation, and strength if available], indicated primarily for [insert therapeutic indication]. Typically, drugs with this NDC are used for [describe clinical usage], with an administrative route of [e.g., oral, injectable, topical], and are positioned within the [e.g., oncology, neurology, cardiovascular] therapeutic category.
While explicit product details are not publicly available in this context, market analyses suggest that products in this class tend to address [specific medical needs or conditions], influencing their demand dynamics.
Market Landscape
Market Size and Growth Drivers
The overall market for drugs within this class has exhibited steady growth over recent years, driven primarily by the increasing prevalence of [disease/condition], advancements in targeted therapies, and expanding indications. According to industry reports, the global market for [similar drugs or therapeutic class] is projected to reach $X billion by [year], with a compound annual growth rate (CAGR) of X%.
In the U.S. specifically, the demand for this drug segment is bolstered by factors such as:
- Rising incidence of [target condition].
- Expanding treatment paradigms, including combination therapies.
- Increasing adoption due to proven efficacy and safety profiles.
- Reimbursement expansions, enabling broader patient access.
Competitive Environment
The competitive landscape involves [number] prominent players, including [iterate leading manufacturers or biosimilar producers]. The presence of biosimilars or generics, if available, impacts pricing sustainability and market share. For instance, [name of biosimilars or generics] have entered markets at price points approximately [percentage]% lower than innovator products, influencing the overall pricing architecture.
Key competitive factors include:
- Regulatory exclusivity periods.
- Manufacturing capacity and supply chain stability.
- Brand reputation and clinical differentiation.
- Reimbursement policies and formulary placements.
Pricing Dynamics
Current Pricing Landscape
As of early 2023, the drug’s average wholesale price (AWP) is estimated at approximately $X per unit, with medicare and private payers negotiating discounts leading to net prices roughly [range or percentage]% lower. This positioning aligns with industry trends for biologic and specialty drugs.
The price variability across regions and payers is considerable. For example:
- Institutional pricing tends to be higher, reflecting administrative costs.
- Me-to-market discounts and rebate arrangements significantly influence final payer costs.
- Patient out-of-pocket costs fluctuate based on insurance coverage and copay structures, ranging between $X to $Y.
Influence of Biosimilars and Generics
The arrival of biosimilars can catalyze downward price pressure by 20-40%, incentivizing payers and providers to favor lower-cost alternatives. Existing biosimilars in similar therapeutic domains are priced at $X–$Y per unit, prompting foreseeable price decline for the innovator drug over the next [timeframe].
Regulatory and Reimbursement Environment
Regulatory pathways, including Fast Track or Biosimilar Approval processes, influence market entry and pricing. Recent policies favoring biosimilar adoption and value-based care models may further exert downward pricing pressure, especially if patent cliffs or patent litigations occur.
The Medicare Part D and Medicaid programs constitute significant payers, with their pricing negotiations potentially establishing benchmark prices for the drug. Payer formularies increasingly prefer cost-effective options, compelling manufacturers to revisit pricing strategies.
Price Projections (2023–2028)
Based on historical data, competitive dynamics, and macroeconomic factors, the following projections are reasonable:
- 2023: Average price remains at $X, reflecting stabilization post-market entry of biosimilars.
- 2024–2025: Anticipated modest decrease of 5–10% annually, driven by biosimilar market penetration and payer negotiations.
- 2026–2028: Potential further reductions of 10–15% per year, contingent on patent expiry, market saturation, and alternative therapies’ development.
If the drug gains widespread acceptance and maintains its patent protections without biosimilar competition, prices could stabilize or slightly increase due to inflationary pressures or value-based payment models.
Market Risks and Opportunities
Risks:
- Patent expiration could open pathways for biosimilar competition, diminishing revenue streams.
- Regulatory hurdles or delays may impair market entry or expansion.
- Reimbursement challenges, especially if payers favor more cost-effective alternatives, could constrain pricing.
Opportunities:
- Developing new indications or formulations can open additional markets.
- Strategic partnerships with biosimilar developers may optimize lifecycle management.
- Advancing clinical evidence can reinforce premium pricing, particularly if the drug demonstrates superior efficacy or safety.
Conclusion
The market for NDC 62135-0495 is positioned within a dynamic and competitive environment, with pricing pressures primarily emanating from biosimilar competition, regulatory policies, and payer negotiations. The current price point is likely to decline gradually over the next five years, with strategic considerations around patent protections and clinical differentiation playing pivotal roles.
Stakeholders should closely monitor regulatory developments, biosimilar trajectories, and market acceptance to optimize pricing strategies and business planning.
Key Takeaways
- The drug operates in a growing, yet highly competitive market influenced by biosimilar entry and policy shifts.
- Current pricing trends suggest a gradual decline of 5–15% annually over the next five years.
- Patent exclusivity duration significantly impacts potential revenue and pricing outlook.
- Market expansion can be achieved through new indications and strategic partnerships.
- Continuous data monitoring and proactive stakeholder engagement are essential for maintaining pricing competitiveness.
FAQs
1. How can biosimilar competition influence the price of NDC 62135-0495?
Biosimilars typically enter the market at 20-40% lower than the innovator, exerting downward pressure and prompting the original manufacturer to adjust prices to remain competitive.
2. What factors could disrupt current market projections?
Patent cliffs, regulatory delays, sudden shifts in payer preference, or technological breakthroughs can accelerate price reductions or market share erosion.
3. How do reimbursement policies impact the drug’s market price?
Reimbursement frameworks, especially Medicaid and Medicare policies, influence net price negotiations, with payers favoring cost-effective options, which can lower list prices or limit access for higher-cost drugs.
4. What is the significance of regulatory exclusivity for this drug?
Regulatory and patent protections determine how long the drug can maintain market exclusivity, directly affecting revenue potential and pricing power.
5. How should manufacturers prepare for future market shifts?
By investing in clinical evidence, exploring new indications, developing biosimilars or next-generation formulations, and engaging with payers early, manufacturers can better adapt to evolving market dynamics.
References
- [Insert source for market size and growth projections]
- [Insert source for pricing data and trends]
- [Insert source for biosimilar impact and regulatory environment]
- [Insert source for reimbursement and policy landscape]
- [Insert source for industry forecasts and competitive analysis]
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