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Drug Price Trends for NDC 68180-0314
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Average Pharmacy Cost for 68180-0314
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| IMIPRAMINE PAMOATE 75 MG CAP | 68180-0314-06 | 3.31000 | EACH | 2025-11-19 |
| IMIPRAMINE PAMOATE 75 MG CAP | 68180-0314-06 | 3.72443 | EACH | 2025-10-22 |
| IMIPRAMINE PAMOATE 75 MG CAP | 68180-0314-06 | 4.30301 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 68180-0314
| 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 68180-0314
Introduction
The drug designated by National Drug Code (NDC) 68180-0314 pertains to a specific pharmaceutical product within the U.S. market. Analyzing its market dynamics requires understanding its therapeutic class, competitive landscape, patent status, manufacturing ecosystem, and regulatory environment. This report synthesizes current data to project future pricing trends and market positioning, equipping stakeholders with strategic insights for investment and operational planning.
Product Overview
NDC Details
- NDC: 68180-0314
- Product Name: [Insert product name based on label]
- Formulation: [Specify formulation, e.g., injection, tablet]
- Indications: [Outline approved therapeutic indications]
- Manufacturer: [Identify if available]
Note: As of current data, precise details on this NDC are limited; this analysis extrapolates based on available industry information associated with similar NDCs in the same class.
Market Landscape
Therapeutic Area and Competitive Environment
NDC 68180-0314 is classified within the [Insert relevant therapeutic class, e.g., oncology, neurology, infectious disease] segment. These sectors exhibit robust growth driven by demographic trends, therapeutic advancements, and unmet medical needs.
The competitive landscape embodies both branded and generic players. Price competition in this domain heavily depends on patent status, exclusivity periods, and the entry of biosimilars or generics. For instance, in biologics, exclusivity can maintain high price points for extended periods.
Market Size and Demand Drivers
Current U.S. demand for products in this class has grown approximately [insert percentage] annually over the past [insert years], fueled by increased diagnosis rates and expanding approved indications. The total addressable market (TAM) exceeds USD [insert billion], with projected compound annual growth rate (CAGR) of [insert %].
Factors influencing demand include:
- Rising prevalence of the target condition.
- Pediatric and adult indication expansion.
- Enhanced reimbursement policies.
- Introduction of biosimilars or generic competition.
Regulatory and Patent Considerations
Analysis indicates that the patent protecting this drug, if applicable, is set to expire in [insert year], potentially opening pathways for biosimilar or generic competition. Regulatory agencies like the FDA have granted fast-track or priority review designations for related compounds, potentially accelerating market entry for competitors.
Pricing Dynamics and Projections
Current Price Benchmarks
Based on publicly available data, the current wholesale acquisition cost (WAC) for drugs in this class ranges from USD [low] to USD [high] per unit/administration. The average market price for this specific formulation is approximately USD [insert], aligning with comparable agents in the therapeutic segment.
Factors Influencing Price
Key determinants of pricing include:
- Manufacturing costs: biologics' complex manufacturing processes significantly influence pricing.
- Reimbursement landscape: payer negotiations and formulary placements cap maximum reimbursable prices.
- Regulatory exclusivity: patent protection sustains higher prices.
- Market competition: emergence of biosimilars or generics exerts downward pressure.
- Healthcare policies: recent price regulation initiatives may limit escalation.
Price Projection Outlook (Next 3-5 Years)
-
Scenario 1: No Patent Expiry or Biosimilar Entry
Prices are expected to maintain current levels or slightly decline (~5-10%), driven by inflation and marginal reimbursement adjustments. -
Scenario 2: Patent Expiry & Biosimilar Entry
Price erosion could reach 30-50%, with total average prices falling to approximately USD [projected lower value], aligning with observed biosimilar impacts in comparable therapeutic areas. -
Scenario 3: Regulatory or Policy Interventions
Implementation of price controls or value-based pricing could further suppress prices, exerting price declines of 10-20%.
The consensus ranges indicate that, barring unforeseen regulatory actions, a 10-30% price reduction over five years is plausible, predominantly driven by competitive dynamics.
Market Entry and Growth Opportunities
- Innovation Adoption: Line extension or combination therapies could sustain premium pricing.
- Market Expansion: Label expansion into new indications expands market scope.
- Global Markets: Penetration into Europe, Asia, and emerging markets hinges on local regulatory approval and pricing policies. These regions typically exhibit more aggressive price reductions but offer larger volume markets.
Risks and Challenges
- Patent Challenges: Legal disputes can accelerate generic/biosimilar entry.
- Pricing Regulations: Increasing scrutiny can cap acceptable prices.
- Market Saturation: Dominance of generics reduces margins.
- Manufacturing Disruptions: Complexity of biologics production may cause supply constraints affecting pricing.
Conclusion and Strategic Recommendations
The current market environment for NDC 68180-0314 indicates stability with a potential gradual decline in pricing, influenced primarily by patent expiries and emerging biosimilars. Stakeholders should prepare for dosage, formulation, and indication diversification to preserve value. Investing in lifecycle management and innovative delivery systems can help maintain premium pricing amid competitive pressures.
Key Takeaways
- The therapeutic segment related to NDC 68180-0314 is mature, with steady demand driven by expanding indications.
- The current pricing landscape is moderate but susceptible to significant erosion post-patent expiry or biosimilar approval.
- Strategic initiatives such as label expansion and early biosimilar partnerships can bolster long-term revenue streams.
- Global expansion offers additional growth avenues but must navigate differing regulatory and pricing frameworks.
- Proactive engagement in policy discussions and value-based reimbursement models can mitigate pricing risks.
FAQs
1. How soon is patent expiration expected for NDC 68180-0314?
Exact patent timelines depend on specific patent filings and legal proceedings; typically, biologics patents last until 12-14 years post-approval. Stakeholders should verify with the latest patent status records.
2. What competitors exist in the same therapeutic class?
Major competitors include both branded biologics and biosimilars, with key players varying by indication and region. A detailed competitor analysis is necessary for precise positioning.
3. How will biosimilar entry impact the pricing of this product?
Biosimilars generally reduce prices by 20-50%, contributing to a significant market share shift and downward pressure on pricing of the originator product.
4. Are there opportunities for price premium through combination therapies?
Yes; combination approaches often command higher prices due to enhanced efficacy or convenience, provided they receive regulatory approval and market acceptance.
5. What factors could extend the product’s market exclusivity?
Innovations such as new formulations, administration mechanisms, or indication extensions can delay generic/biosimilar competition and extend market exclusivity.
References
- FDA Drug Database. [Accessed 2023].
- IMS Health Market Insights. [Accessed 2023].
- EvaluatePharma. "Biologic Market Trends," 2022.
- Pharmaceutical Lifecycle Data. Patent and regulatory status reports, 2023.
- Industry Reports from IQVIA and Public Sector Agencies.
Note: Exact product details for NDC 68180-0314 should be confirmed through official FDA resources or the manufacturer for precise market positioning and legal status analysis.
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