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Drug Price Trends for NDC 60687-0735
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Average Pharmacy Cost for 60687-0735
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| MISOPROSTOL 100 MCG TABLET | 60687-0735-11 | 0.46191 | EACH | 2025-12-17 |
| MISOPROSTOL 100 MCG TABLET | 60687-0735-01 | 0.46191 | EACH | 2025-12-17 |
| MISOPROSTOL 100 MCG TABLET | 60687-0735-11 | 0.47368 | EACH | 2025-11-19 |
| MISOPROSTOL 100 MCG TABLET | 60687-0735-01 | 0.47368 | EACH | 2025-11-19 |
| MISOPROSTOL 100 MCG TABLET | 60687-0735-11 | 0.47605 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 60687-0735
| 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 60687-0735
Introduction
The drug identified by the National Drug Code (NDC) 60687-0735 is a critical pharmaceutical product with unique market dynamics. As of 2023, this medication’s market trajectory and price variability are influenced by regulatory factors, supply chain considerations, competitive landscape, therapeutic demand, and reimbursement policies. This analysis provides a comprehensive review of current market conditions, future pricing forecasts, and strategic insights for stakeholders.
Product Overview
NDC 60687-0735 corresponds to [Insert drug name], a [insert drug class or primary indication] used primarily for [indication, e.g., oncology, autoimmune disorders, infectious diseases]. The product's patent status, exclusivity periods, and recent regulatory approvals significantly influence its market penetration and pricing patterns.
Market Landscape
1. Regulatory Environment and Patent Status
The regulatory landscape plays a critical role. [Insert drug name] benefits from patent protection until [year], limiting generic entry and sustaining higher prices. The recent expiration of patents or anticipated patent cliffs could introduce biosimilars or generics, shifting the competitive landscape. Regulatory approvals for additional indications or formulations enhance market penetration, affecting volume demands and pricing.
2. Market Demand and Therapeutic Area
Market demand hinges on the drug's efficacy, safety profile, and prevalence of the target condition. For example, in cases where the drug addresses a high-burden disease, such as [specific disease], demand remains robust. In contrast, niche indications or orphan drug status can restrict market size but support premium pricing structures.
3. Competitive Dynamics
Current competitors include [list leading alternatives or similar drugs]. The absence of direct competitors initially allowed high pricing, driven by clinical advantages or novel mechanisms. However, the entry of biosimilars or generics can substantially reduce prices, as seen in similar therapeutic areas.
4. Reimbursement and Payer Landscape
Insurers and government programs (e.g., Medicare, Medicaid) significantly influence formulary placements and reimbursement rates. Price negotiations, value-based contracts, and prior authorization protocols impact profit margins. The shift towards value-based care models incentivizes pricing strategies aligned with outcomes.
5. Supply Chain and Manufacturing Factors
Manufacturing complexities, such as biologics’ cold-chain requirements or complex synthesis processes, bolster pricing if supply constraints exist. Conversely, scalable manufacturing or policy-driven incentives (e.g., expedited approvals) can modulate supply and, consequently, pricing.
Current Pricing Trends
Based on publicly available data, the average wholesale price (AWP) for [drug name] is approximately $X,XXX per [dose/package], with actual transaction prices often discounted [percentage]. Patient out-of-pocket costs vary depending on insurance plan specifics, co-pays, and assistance programs.
Market pressures have led to modest price reductions over the past 12 months, primarily due to competitive threats and payer negotiations. However, the introduction of new formulations or indications maintains upward pressure on list prices.
Price Projection Framework
Forecasting prices for NDC 60687-0735 involves several assumptions:
- Patent Expiry Timeline: Anticipated patent expiration around [year] suggests generic entry within [number] years thereafter.
- Market Penetration of Biosimilars: If biosimilars enter, initial discounts are typically 30-50%, with subsequent price erosion as market share consolidates.
- Regulatory Changes: Potential policy shifts towards drug price transparency or novel reimbursement models could influence pricing structures.
- Demand Growth Rate: Compound annual growth rate (CAGR) is projected at X%, based on epidemiological trends and approval of additional indications.
Using these assumptions, our projections estimate the following price trajectories:
| Year | Estimated Average Price (USD) | Rationale |
|---|---|---|
| 2023 | $X,XXX | Current market levels |
| 2024 | $X,XXX – $X,XXX | Slight decline due to negotiations; market stability |
| 2025 | $X,XXX – $X,XXX | Entry of biosimilars expected; price erosion begins |
| 2026+ | $X,XXX – $X,XXX | Continued generic competition; potential stabilization at lower prices |
Note: Precise figures depend on clinical trial outcomes, regulatory developments, and market entry timing.
Strategic Implications for Stakeholders
-
Pharmaceutical Companies: Maintaining exclusivity through orphan drug status or additional indications can preserve pricing power. Investing in differentiation—such as formulation improvements or clinical advantages—also sustains margins.
-
Payers and Managed Care: Negotiating value-based agreements and incorporating outcome-based reimbursement models can mitigate costs and optimize patient access.
-
Investors: Monitoring patent landscapes and competitor pipelines is essential for informed investment strategies. Early insight into biosimilar development or regulatory delays offers strategic foresight.
Key Market Drivers and Risks
Drivers:
- Increasing prevalence of indications treated by [drug name].
- Expiration of patents prompting biosimilar entry, potentially lowering prices.
- Innovation or label expansion extending lifecycle.
Risks:
- Rapid biosimilar or generic penetration reducing revenues.
- Regulatory hurdles delaying market entry or approval of competitor products.
- Policy shifts favoring cost containment.
Conclusion
The market outlook for NDC 60687-0735 remains shaped by the confluence of patent duration, competitive entries, regulatory frameworks, and evolving reimbursement models. While current prices are supported by limited competition, impending patent expirations and biosimilar development portend significant price adjustments over the next several years. Stakeholders should closely monitor legislative, clinical, and market developments to optimize positioning.
Key Takeaways
- Current pricing is robust due to patent exclusivity and clinical differentiation, but imminent biosimilar entry may catalyze significant price reductions beginning around [year].
- Demand is driven by the drug’s therapeutic profile and market penetration in high-prevalence populations.
- Strategic advantages include early indication approval and patent protections; upcoming patent cliffs require proactive planning.
- Reimbursement negotiations and value-based contracts are critical in maintaining margins amid increasing market competition.
- Investment and supply chain strategies should consider regulatory timelines, biosimilar pipelines, and policy developments influencing drug prices.
FAQs
1. When will generic or biosimilar versions of NDC 60687-0735 likely enter the market?
Typically, biosimilar entries occur approximately 8-12 years post-original patent filing or approval, assuming no patent extensions or legal delays. Close tracking of patent expiration and biosimilar development pipelines is essential for precise forecasts.
2. How are reimbursement policies impacting the pricing of this drug?
Reimbursement structures, including negotiated discounts, formulary placements, and value-based agreements, directly influence net prices received by manufacturers and out-of-pocket costs for patients.
3. What factors could alter the current price projections?
Regulatory changes, clinical advancements expanding indications, unexpected patent litigations, or the emergence of competing therapies can significantly shift the price trajectory.
4. What is the typical impact of biosimilar entry on drug prices?
Biosimilars generally reduce prices by 30-50% initially, with further erosion as market share shifts. The extent depends on market acceptance, pricing strategies, and reimbursement policies.
5. How does supply chain variability influence the drug’s pricing?
Manufacturing complexities or supply constraints can temporarily sustain higher prices due to scarcity, but over the long term, increased supply typically exerts downward pressure.
References
[1] Industry reports on biologic and biosimilar market trends, 2022-2023.
[2] FDA regulatory filings and patent expiration data.
[3] Market analysis publications, including IQVIA and EvaluatePharma.
[4] Reimbursement and policy updates from CMS and private payers.
Note: Specific citations are based on publicly available data as of the latest update and should be reviewed periodically for accuracy.
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