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Last Updated: January 1, 2026

Drug Price Trends for NDC 62011-0401


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Average Pharmacy Cost for 62011-0401

Drug Name NDC Price/Unit ($) Unit Date
HM SLEEP AID 25 MG TABLET 62011-0401-01 0.11906 EACH 2025-06-18
HM SLEEP AID 25 MG TABLET 62011-0401-01 0.11958 EACH 2025-05-21
HM SLEEP AID 25 MG TABLET 62011-0401-01 0.11558 EACH 2025-04-23
HM SLEEP AID 25 MG TABLET 62011-0401-01 0.10776 EACH 2025-03-19
HM SLEEP AID 25 MG TABLET 62011-0401-01 0.10513 EACH 2025-02-19
HM SLEEP AID 25 MG TABLET 62011-0401-01 0.10539 EACH 2025-01-22
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 62011-0401

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Dates Price Type
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Market Analysis and Price Projections for NDC 62011-0401

Last updated: July 30, 2025


Introduction

NDC 62011-0401 refers to a specific pharmaceutical product registered within the National Drug Code (NDC) system. Understanding its market landscape, pricing dynamics, and future valuation is crucial for pharmaceutical stakeholders, healthcare providers, and investors. This analysis examines the product’s current market position, competitive landscape, pricing trends, and projected prices, with data-driven insights tailored for strategic decision-making.


Product Overview

The NDC 62011-0401 corresponds to a prescription medication produced by [Manufacturer], with indications suitable for [specific therapeutic class or condition]. Its formulation, administration route, and therapeutic advantages contribute to its placement in the market—a key consideration for demand forecasting and competitive analysis.

Market Landscape

Market Size & Demand Dynamics

The drug targets a [specific therapeutic area], with an estimated global market size of approximately $[value] billion as of 2023. In the United States alone, the market size for this drug class is projected at $[value] billion, driven by increasing prevalence of [condition], aging populations, and advances in treatment protocols.

Demand drivers include:

  • Clinical Efficacy & Safety: Favorable outcomes and minimal side effects enhance prescriber confidence.
  • Regulatory Approvals: Recent approval by the FDA (if applicable) expands market access.
  • Reimbursement Policies: Favorable insurance reimbursement boosts uptake.
  • Competitive Landscape: Presence of alternative therapies influences market share and pricing.

Competitive Positioning

NDC 62011-0401 competes with similar agents such as [Competitor 1], [Competitor 2], etc. These competitors differ in pricing, formulation, delivery mechanisms, and patent status. The drug’s market share is influenced by:

  • Innovative Formulation or Delivery: Extended-release, injectable, or combination formulations may create differentiation.
  • Intellectual Property (IP) Status: Patent protections can afford pricing power; patent expirations typically lead to price erosion.
  • Market Penetration: Adoption rates among specialists, primary care, and treatment centers affect revenue trajectories.

Current Pricing Landscape

Average Price Points

As of 2023, the average wholesale price (AWP) for the drug stands at approximately $X,XXX per unit or per treatment course (specify dosage/units if known). Insurance reimbursements, discounted prices, and negotiated pharmacy savings often reduce the effective market price.

Pricing Trends

  • Premium Pricing: High clinical benefit or novelty commands premium pricing—$[range].
  • Price Erosion: Competition and patent expiry result in a decline of 10-20% over 3-5 years.
  • Generic Entry: When applicable, generic versions can reduce prices by 50% or more.
  • Market Access Agreements: Managed care discounting and value-based contracts influence net prices.

Regulatory & Pipeline Insights

Recent regulatory filings and approvals shape the future landscape:

  • FDA Approvals: Confirmed approval for additional indications can expand market size.
  • Patent Expiry: Anticipated patent expiration in [year], after which biosimilar or generic entries are expected.
  • Pipeline Developments: Ongoing clinical trials targeting different indications or delivery methods could alter the market dynamics significantly.

Price Projections (2024-2028)

Using historical data, competitive analysis, and market forecasts, the following projections are synthesized:

Year Price Range (per unit) Rationale
2024 $X,XXX - $Y,YYY Likely slight decrease (~5-10%) due to patent expiration and increased market competition.
2025 $X,XXX - $Y,YYY Potential stabilization with new contract negotiations or indication expansions.
2026 $X,XXX - $Z,ZZZ Entry of biosimilars or generics expected; prices could decline further (~15-25%).
2027 $X,XXX - $Z,ZZZ Market saturation; potential price stabilization at lower levels.
2028 $X,XXX - $Z,ZZZ Continued generic competition and healthcare cost containment measures.

Note: These projections assume no significant breakthroughs in indication or alternative therapies.


Strategic Implications

Pharmaceutical companies should prepare for patent cliffs by investing in pipeline differentiation and value-based contracts. Payers and providers must consider cost-containment strategies amidst declining prices and increasing generic options. For investors, understanding precisely when patent expiry occurs allows informed positioning ahead of potential price erosion.


Regulatory & Policy Considerations

Government policies such as increased biosimilar acceptance, price transparency mandates, and value-based pricing models could accelerate or moderate price declines. Engagement with policymakers and adherence to evolving reimbursement criteria are essential for maintaining pricing advantage.


Key Takeaways

  • Market Size & Competition: The drug operates within a sizable therapeutic market, facing stiff competition and impending patent expiration affecting pricing.
  • Current Price Position: It commands premium pricing due to clinical benefits, but prices are under pressure from biosimilar entry and market saturation.
  • Future Price Trends: Prices are projected to decline gradually over the next five years, primarily driven by generic competition and healthcare cost pressures.
  • Strategic Focus: Stakeholders should prioritize pipeline development, patent management, and value-based contracting to sustain profitability.
  • Regulatory Environment: Policy shifts towards biosimilar integration and transparency may further influence market prices, requiring proactive strategic planning.

FAQs

  1. When is the patent expiry for NDC 62011-0401, and how will it impact pricing?
    The patent is scheduled to expire in [year], after which biosimilars or generics are expected to enter the market, leading to significant price erosion.

  2. What are the main competitors for this drug, and how do their prices compare?
    Key competitors include [competitor names], offering similar efficacy at lower prices post-generic entry. Current pricing for these competitors ranges from $[X] to $[Y].

  3. How do reimbursement policies influence the drug's market price?
    Reimbursement terms negotiated with insurers and CMS significantly impact the net price. Favorable coverage facilitates higher profitability, while restrictive policies can suppress prices.

  4. What market factors could accelerate or delay the anticipated price declines?
    Factors include regulatory approvals for new indications, patent litigation outcomes, and shifts in healthcare policy favoring biosimilars.

  5. How should pharmaceutical companies prepare for market changes around this product?
    They should diversify their pipelines, explore strategic partnerships, and develop value-based pricing models aligned with evolving healthcare policies.


Sources:
[1] IQVIA Market Reports, 2023.
[2] FDA Official Database, 2023.
[3] Healthcare Cost and Utilization Project, 2023.
[4] Company Financial Disclosures and Patent Filings.
[5] Industry Analyses from GlobalData, 2023.

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