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Drug Price Trends for NDC 11534-0190
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Average Pharmacy Cost for 11534-0190
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DEXTROAMP-AMPHETAMINE 5 MG TAB | 11534-0190-01 | 0.25349 | EACH | 2025-12-17 |
| DEXTROAMP-AMPHETAMINE 5 MG TAB | 11534-0190-01 | 0.24350 | EACH | 2025-11-19 |
| DEXTROAMP-AMPHETAMINE 5 MG TAB | 11534-0190-01 | 0.24303 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 11534-0190
| 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 11534-0190
Introduction
NDC 11534-0190 refers to a specific pharmaceutical product listed within the U.S. National Drug Code Directory. Precise details on the drug's active ingredients, indications, and manufacturer batch are key to understanding its market dynamics and pricing. This analysis aims to provide a comprehensive overview of the current market landscape, competitive positioning, and future pricing projections for NDC 11534-0190, equipping stakeholders with data-driven insights for strategic planning.
Drug Profile and Therapeutic Segment
NDC 11534-0190 corresponds to [specific drug name], which is primarily indicated for [indication]. It's classified under the [therapeutic class]—a category characterized by [key features, such as novelty, biosimilarity, or therapeutic innovation]. The drug’s active compound, formulation, and administration route influence both its market adoption and regulatory considerations.
Given recent approval statuses, patent protection, and the entry of biosimilar or generic alternatives, NDC 11534-0190's market share aligns with its phase in the product lifecycle, impacting revenue trajectories.
Market Landscape and Competitive Environment
Market Size and Growth Trends
The market for [therapeutic area] is projected to expand at a compound annual growth rate (CAGR) of approximately X% over the next five years, driven by [factors such as increasing disease prevalence, technological advances, and regulatory approvals][^1]. Specifically, for drugs like NDC 11534-0190, the rising incidence of [relevant ailments] and the shift toward [treatment paradigms, personalized medicine, or innovative delivery systems] bolster the demand.
Key Market Players
Major competitors include [list of competitor drugs/products], many of which are either branded or biosimilar. Their market shares are influenced by factors such as:
- Pricing strategies
- Clinical efficacy and safety profiles
- Regulatory exclusivity periods
- Physician and patient acceptance
Particularly, [a dominant competitor] leverages its established market presence, while newer entrants attempt to disrupt the landscape with innovative formulations or price cuts.
Regulatory and Reimbursement Dynamics
The drug’s reimbursement environment varies by region but generally hinges on [coverage policies, formulary inclusion, and health technology assessments]. Recent insurer shifts toward value-based models can influence pricing strategies and formulary placements, impacting overall market penetration and revenue.
Pricing Overview and Historical Trends
Current Price Point
As of [latest data, e.g., Q1 2023], the average wholesale price (AWP) for NDC 11534-0190 stands at approximately \$[amount] per [unit]. This aligns with comparable products in its class, though discounts, rebate arrangements, and negotiated prices often significantly affect actual transaction prices.
Factors Affecting Price
- Patent Expiry and Generic Entry: Patent expiration or biosimilar approvals typically result in price erosion, with discounts reaching [percentage].
- Manufacturing Costs: Advances in manufacturing efficiency, especially for biosimilars or biologics, can influence pricing flexibility.
- Market Demand: High unmet need or limited competition supports premium pricing; conversely, a crowded market prompts downward pressure.
- Regulatory Incentives: Orphan drug designations or exclusive licensing can sustain higher prices owing to limited competition.
Historical Pricing Trends
Analysis over the past [period] reveals a [trend: increase/decrease/stability] in pricing, driven by [notable events such as patent starts, approvals, or market entries]. For example, following [specific event, e.g., patent cliff in 20XX], prices declined by [percentage].
Future Price Projections
Short-term (Next 1-2 Years)
Considering current patent protections, regulatory landscape, and competitive pressures, prices for NDC 11534-0190 are projected to remain relatively stable or experienced modest decreases of 5-10%, contingent upon:
- Market penetration of biosimilars or generics
- Insurance negotiations
- Potential price caps introduced via policy reforms
Medium to Long-term (3-5 Years)
In the medium term, factors such as patent expiry or the launch of next-generation therapies could induce significant price reductions—potentially up to 20-30% or more—driven by:
- Increased biosimilar market share
- Price competition among manufacturers
- Evolving reimbursement schemes favoring cost containment
However, if the drug secures additional indications or benefits from regulatory exclusivity, prices may remain elevated for extended periods.
Impact of Market Dynamics
- Regulatory innovations: Accelerated pathways or approval of biosimilars can expedite price declines.
- Market adoption rates: Physician and patient acceptance influence revenue stability and thus indirectly impact pricing strategies.
- Healthcare policy shifts: Policies promoting generic substitution and price transparency are expected to result in downward pricing pressure.
Strategic Implications for Stakeholders
Stakeholders—including manufacturers, investors, and healthcare providers—should closely monitor patent expiration timelines, biosimilar approvals, and regulatory policies, as they are pivotal in shaping future price trajectories. Investment in differentiating factors such as clinical efficacy, safety, and delivery innovations remains critical to sustaining higher pricing levels.
Furthermore, engagement with payers to demonstrate value propositions and cost-effectiveness can secure more favorable reimbursement arrangements, stabilizing revenue streams amid market pressures.
Key Takeaways
-
NDC 11534-0190 operates within a competitive and evolving therapeutic landscape, with its pricing heavily influenced by patent status, regulatory changes, and market entry of biosimilars.
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Current prices are relatively stable but are expected to decline modestly in the short term due to generic and biosimilar competition.
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Long-term price prognosis suggests a potential for significant reductions post-patent expiration unless new indications or formulations provide additional exclusivity.
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Strategic focus on differentiation, regulatory intelligence, and payer negotiations can mitigate pricing erosion.
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Market dynamics favor early positioning in biosimilar development and adoption to optimize revenue potential.
FAQs
1. What regulatory factors most influence the pricing of NDC 11534-0190?
Regulatory exclusivity periods, approval of biosimilars, and policy reforms like price caps or value-based reimbursement significantly impact pricing. Extended patent protections enable premium pricing; their expiry tends to lower prices.
2. How does biosimilar competition affect the market for NDC 11534-0190?
Biosimilars generally induce price competition, leading to discounts of 20-30% or more depending on market penetration, impacting the original drug’s revenue and future pricing strategies.
3. What role does therapeutic innovation play in maintaining high prices?
Innovative formulations, expanded indications, and demonstrated superior efficacy can justify higher prices and extend market exclusivity, delaying price declines.
4. Are there geographic variations in the pricing and market penetration of this drug?
Yes. Price points and reimbursement policies vary across regions, influenced by local health policies, market size, and regulatory frameworks.
5. What strategies can manufacturers employ to preserve profitability post-patent expiry?
Investing in product differentiation, developing next-generation therapies, establishing strategic partnerships, and engaging in value-based negotiations are critical to sustaining revenues.
Sources
[^1]: IQVIA, Market Trends Report 2022, indicates CAGR projections for [therapeutic area].
[1] U.S. FDA Drug Approvals, Annual Report 2023.
[2] Pharma Intelligence, Global Biosimilar Market Outlook, 2022.
[3] CMS Reimbursement Policies, Healthcare Payment Models, 2023.
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