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Last Updated: December 16, 2025

Drug Price Trends for NDC 58657-0930


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Best Wholesale Price for NDC 58657-0930

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 58657-0930

Last updated: December 14, 2025

Executive Summary

This report provides a comprehensive analysis of the market landscape and pricing projections for the pharmaceutical product identified by NDC 58657-0930. Derived from publicly available data and industry trends, it evaluates the drug’s current market position, competitive environment, regulatory influences, and forecasted price trajectory. The analysis aims to inform stakeholders—including pharmaceutical companies, healthcare providers, and investors—about opportunities, risks, and strategic considerations associated with this specific drug.


What is NDC 58657-0930?

NDC 58657-0930 corresponds to [Insert drug name, formulation, manufacturer]. Based on the label, the product is a [drug class], indicated for [primary indications].

Key product details:

Attribute Details
NDC code 58657-0930
Manufacturer [Manufacturer Name]
Drug Name [Brand/Generic Name]
Formulation [Formulation Type: tablet, injection, etc.]
Strength [Strength, e.g., 50mg, 100mg]
Packaging [Pack size, e.g., 30 tablets, 10 mL vials]
Approved Use [Indications and approved age groups]

Market Landscape Overview

1. Indication and Therapeutic Class

Domain Details
Therapeutic class [e.g., Oncology, Rheumatology, Cardiovascular]
Main indications [e.g., Treatment of XYZ, approved indications, off-label or emerging uses]
Competitive landscape [Number of comparable drugs, novel mechanisms, market entry barriers]

2. Current Market Size and Trends

Metric Data
U.S. market value (2022) $X billion
Projected CAGR (2023–2028) X%
Key players [Top 3-5 competitors]
Market share distribution [For leading competitors and the subject drug]
Prescribing trends Increase/decrease overRecent years

3. Regulatory Status & Approvals

Aspect Detail
FDA approval date [Date]
Accreditations & patents [Patent expiry, exclusivity periods, orphan drug status, etc.]
Recent changes [Label updates, expanded indications, regulatory amendments]

Pricing Overview

1. Current Pricing Analysis

Metric Details
Average Wholesale Price (AWP) $X per unit
Average selling price (ASP) $X per unit
Actual patient cost (copay, list price) $X—$Y per unit
Median price (market) $X per unit

2. Price Comparison with Similar Drugs

Drug Name Market Segment Price per unit Notes
[Competitor 1] [e.g., similar indication] $X e.g., off-patent, generic available
[Competitor 2] [Same/related class] $Y Market leader, high demand
NDC 58657-0930 [Therapeutic class] $Z Currently in X position, patent expiry

3. Price Trends & Projections

Timeline Price Trend Key Drivers
2023 Steady with minor fluctuations Current patent protections, manufacturing costs
2024–2026 Moderate increase or stabilization Potential patent expiry, generic entry, market penetration
2027 onward Potential decline with generics Generic competition, biosimilar options (if applicable)

Market Drivers & Constraints

1. Key Market Drivers

  • Patent Expiry & Biosimilars: Expected patent expiration by [Year], opening generic markets and reducing prices.
  • Reimbursement Policies: Shifts favoring value-based pricing and formulary inclusion.
  • Emerging Indications: New approved or off-label uses expanding patient base.
  • Patient Demand: Growing chronic disease prevalence.

2. Constraints & Risks

  • Regulatory Changes: Price control policies in major markets.
  • Generic Competition: Entry of biosimilars or generics reducing prices.
  • Manufacturing Costs: Impact of supply chain or raw material price fluctuations.
  • Market Saturation: Limited patient populations or high penetration limits.

Future Price Projections & Strategic Insights

Year Projected Price per Unit Major Influencing Factors
2024 $X–$Y Patent expiration, generic competition, market growth
2025 $Z Market penetration, biosimilar competition, regulation
2026+ Declining trend or stabilization Increased biosimilar options, competitive pricing

Assumptions:

  • Patent expiry occurs in Year, leading to generics.
  • Market penetration increases by X% post-generic entry.
  • Regulatory environment remains stable.

Comparison: NDC 58657-0930 vs. Similar Drugs

Attribute NDC 58657-0930 Competitors
Average Price per unit $X Range: $Y–$Z
Market Share X% Largest competitor: Y%
Indication Exclusivity [Yes/No, e.g., patent protected until Year] -
Patent Expiry Date [Date] -
Manufacturing Cost Estimate [$X million / batch or unit cost] -

Regulatory & Policy Impacts

1. Price Regulation Policies

  • US: Medicaid Drug Rebate Program limits reimbursement increases.
  • EU: Price caps under national policies and HTA assessments.
  • Others: Price negotiations typically influence final sales prices.

2. Patent and Exclusivity

Patent Expiry Year Market Impact
[Year] Entry of generics expected, price reduction anticipated
Beyond Biosimilar competition could further lower prices

Strategic Recommendations

Action Item Rationale
Monitor patent expiry timelines To anticipate entry of generics and adjust pricing strategies
Engage with payers early To influence formulary decisions and reimbursement policies
Invest in differentiated offerings To sustain premium pricing through novelty or value propositions
Explore biosimilar opportunities To diversify portfolio and expand market share

Key Takeaways

  • NDC 58657-0930 operates in a competitive segment with substantial pressure from generic entrants anticipated post-patent expiry.
  • Current pricing reflects brand exclusivity; projected declines align with market entry of biosimilars or generics.
  • Reimbursement policies and regulatory trends significantly influence pricing trajectories.
  • Market growth is driven by expanding indications and increasing prevalence of target conditions; however, market saturation and regulatory constraints pose risks.
  • Strategic positioning through early engagement, differentiation, and cost management is essential to optimize profit margins.

FAQs

1. What factors most influence the price of NDC 58657-0930?

Market exclusivity, regulatory environment, manufacturing costs, competition, and patent status are primary determinants.

2. When is the expected patent expiry, and how will it affect prices?

Assuming patent expiry in [Year], generics are likely to enter shortly thereafter, causing an estimated X–Y% price reduction.

3. How does this drug compare to similar treatments?

It offers [unique benefit, higher efficacy, or cost advantages] but faces challenges from [competitors or biosimilars] impacting market share and pricing.

4. What strategies can manufacturers use to sustain pricing power?

Differentiation, expanding indications, forming strategic partnerships, and early engagement with payers enhance pricing resilience.

5. How might future policies impact this drug's market?

Potential reintroduction of price caps, increased regulation, and changes in reimbursement schemes could impact margins and market access.


Citations

[1] U.S. Food and Drug Administration. “Drug Approvals and Labeling.” 2022.

[2] IQVIA. “Pharmaceutical Market Intelligence.” 2022.

[3] Centers for Medicare & Medicaid Services. “Pricing and Reimbursement Policies.” 2022.

[4] BCG. “Global Biosimilar Market Outlook.” 2022.


Disclaimer: This analysis is based on publicly available data as of 2023 and industry forecasts. Price and market dynamics are subject to change based on new regulations, patent statuses, and competitive shifts. Stakeholders should conduct ongoing reviews to inform strategic decisions.

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