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Drug Price Trends for NDC 58657-0930
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Average Pharmacy Cost for 58657-0930
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| BACLOFEN 5 MG TABLET | 58657-0930-01 | 0.10217 | EACH | 2025-12-10 |
| BACLOFEN 5 MG TABLET | 58657-0930-05 | 0.10217 | EACH | 2025-12-10 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 58657-0930
| 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 58657-0930
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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