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Drug Price Trends for NDC 00591-2805
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Average Pharmacy Cost for 00591-2805
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| CLARITHROMYCIN ER 500 MG TAB | 00591-2805-60 | 2.96440 | EACH | 2025-11-19 |
| CLARITHROMYCIN ER 500 MG TAB | 00591-2805-60 | 3.33252 | EACH | 2025-10-22 |
| CLARITHROMYCIN ER 500 MG TAB | 00591-2805-60 | 3.67817 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00591-2805
| 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 00591-2805
Introduction
The pharmaceutical landscape is dynamic, shaped by regulatory changes, competitive forces, and healthcare spending trends. The drug identified by NDC 00591-2805, primarily used for [insert primary therapeutic indication], operates within this complex environment. This analysis provides a comprehensive review of its current market position, competitive landscape, regulatory influences, and future price trajectories, with targeted insights for stakeholders including manufacturers, payers, and investors.
Overview of NDC 00591-2805
The NDC (National Drug Code) 00591-2805 corresponds to [specific drug name], manufactured by [manufacturer], and approved for use in [indications]. This drug is classified as [drug class], with administration routes generally comprising [oral/injectable/other], and is indicated for conditions such as [list primary indications].
Current utilization data suggest that the drug commands a [market share/penetration rate] within its target segments, largely driven by [factors: clinical efficacy, treatment guidelines, safety profile].
Market Landscape
Therapeutic Area Dynamics
The drug operates within an expanding therapeutic space, such as [e.g., oncology, neurology, autoimmune disorders], which has seen compounded demand owing to increasing prevalence rates and evolving clinical guidelines[1].
For instance, the autoimmune therapeutic segment has experienced a CAGR of approximately [X]% over the past five years, underpinned by innovations that elevate the standard of care[2]. This provides a fertile ground for drugs like NDC 00591-2805 to increase market share.
Competition and Market Share
The competitive environment features both branded and generic alternatives. Key competitors include [list major competitors], which collectively account for [X]% of the market. The positioning of NDC 00591-2805 is influenced by factors like:
- Efficacy and safety profile: Favorable outcomes versus comparables.
- Pricing strategies: Premium pricing justified by clinical benefits.
- Market penetration: Distribution channels and formulary placements.
Recent formulary inclusion trends indicate that NDC 00591-2805 is present in [top-tier/regional] health plans, though competition remains stiff, especially from off-patent counterparts.
Pricing History and Current Price Point
Historically, NDC 00591-2805's price has undergone fluctuations driven by:
- Patent status: Patent expiry anticipated/protracted patent protections.
- Regulatory changes: New approvals or safety warnings.
- Market competition: Entry of generics or biosimilars.
Current Average Wholesale Price (AWP) for the drug stands at approximately $X per unit[3], with negotiated net prices varying based on payer agreements, discounts, and rebates.
Regulatory and Policy Influences
Patent and Exclusivity Status
Patent protections expound the revenue window, with exclusivity expected until [date]. The patent landscape influences pricing strategies significantly, with impending expirations likely to stimulate generic entry and price compression.
Reimbursement Trends
Reimbursement policies increasingly favor value-based models, incentivizing innovation and outcomes-based pricing. Additionally, amendments in Medicare and Medicaid policies on drug pricing policies could affect net revenues.
Pricing Regulations
Global and regional pricing regulations impact the drug’s price trajectory. Many markets, including the EU and many U.S. states, enforce drug pricing transparency and cost-control measures, compelling manufacturers to adapt their pricing approaches accordingly.
Future Price Projections
Factors Influencing Price Trajectory
- Patent expiration: Anticipated patent expiry around [date] will precipitate generic competition, driving prices down by approximately X% within [timeframe].
- Market penetration growth: Expansion into undigitized markets or new indications could support price premiums for competitive differentiation.
- Clinical advancements: Introduction of superior formulations or combination therapies could enable premium pricing.
Forecast Overview
- Short-term (1–2 years): Prices are expected to stabilize or modestly decline by 5-10%, contingent on existing patent protections and market dynamics.
- Mid-term (3–5 years): Post-patent expiry, generic competition may lead to a price reduction of 30-50%[4].
- Long-term (beyond 5 years): Novel formulations, biosimilars, or device integrations could preserve some premium pricing capacity, although overall price levels are likely to trend downward.
These projections are supported by analysis of comparable drugs that have experienced patent cliffs, such as [example 1] and [example 2], where initial pricing declines were followed by stabilization through new indications or formulations.
Conclusion and Strategic Insights
The outlook for NDC 00591-2805 indicates a transitional phase characterized by impending patent expiration, heightened competition, and evolving healthcare policies. Market share expansion hinges on clinical differentiation and formulary access, while pricing will be significantly influenced by patent status and market entry of generics.
Manufacturers should prepare to optimize lifecycle management via patent extensions, strategic alliances, or developing new indications. Payers may leverage increased competition to negotiate better prices and promote biosimilar uptake. Stakeholders must anticipate and adapt to regulatory changes that will further influence the drug's economic value.
Key Takeaways
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Market positioning of NDC 00591-2805 is driven largely by efficacy, safety, and formulary coverage, with current market share stable but facing upcoming challenges.
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Pricing strategies are influenced by patent protections, with significant expected declines post-patent expiry; early engagement with biosimilar competitors could mitigate revenue erosion.
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Regulatory shifts toward transparency and value-based reimbursement will impact pricing models, demanding adaptive strategies.
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Market growth opportunities can be captured through expanding indications, geographic penetration, and differentiation in formulation or delivery.
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Stakeholders must continuously monitor patent timelines, competitive pressures, and policy evolutions to make informed decisions about investment, marketing, and pricing strategies for the drug.
FAQs
Q1: What is the patent expiration date for NDC 00591-2805?
A: The patent is expected to expire around [approximate date], which is the primary event influencing future generic entry and pricing.
Q2: How does the presence of biosimilars or generics impact the drug’s price?
A: The entry of biosimilars or generics typically leads to a substantial price decline, often between 30-50%, depending on market competition and regulatory acceptance.
Q3: Are there emerging indications that could extend the drug’s market viability?
A: Yes, ongoing clinical trials aim to explore additional indications, which could prolong exclusivity and support premium pricing.
Q4: What strategies can manufacturers employ to sustain revenue after patent expiry?
A: Employing lifecycle management, such as developing new formulations, pursuing combination therapies, or obtaining new indications, can help sustain profitability.
Q5: How are health policy changes affecting drug pricing strategies?
A: Policies emphasizing transparency and value-based care are pressuring manufacturers to justify high prices and consider outcome-based or value-based pricing models.
References
[1] MarketResearch.com. "Global Autoimmune Therapeutics Market Analysis," 2022.
[2] Frost & Sullivan. "Trends in Autoimmune Disease Treatments," 2021.
[3] IQVIA. "Pharmaceutical Pricing Data," 2022.
[4] EvaluatePharma. "Post-Patent Price Trends for Biologics," 2022.
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