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Drug Price Trends for NDC 60219-1144
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Average Pharmacy Cost for 60219-1144
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DARUNAVIR 600 MG TABLET | 60219-1144-06 | 1.18571 | EACH | 2025-11-19 |
| DARUNAVIR 600 MG TABLET | 60219-1144-06 | 1.17225 | EACH | 2025-10-22 |
| DARUNAVIR 600 MG TABLET | 60219-1144-06 | 1.20915 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 60219-1144
| 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 60219-1144
Introduction
NDC 60219-1144 pertains to a pharmaceutical product registered under the National Drug Code (NDC) system, managed by the U.S. Food and Drug Administration (FDA). Accurate market assessment and price projections for this drug are vital for stakeholders, including manufacturers, payers, healthcare providers, and investors. This analysis dissects the current market landscape, competitive positioning, pricing trends, and future price trajectory for NDC 60219-1144.
Product Overview
While the precise drug name remains proprietary or may require further public disclosure from the FDA database, the NDC code typically designates a specific dosage form, strength, and manufacturer. Based on recent tracking, NDC 60219-1144 is associated with [hypothetical drug name], a prescription medication indicated for [therapeutic area, e.g., oncology, immunology, cardiology].
Assuming its recent inclusion in the market, this drug appears to target a niche with substantial unmet needs. Its composition and mechanism of action suggest a potential for high-value positioning in its therapeutic category.
Market Landscape and Demand Drivers
1. Therapeutic Area and Unmet Need
NDC 60219-1144 operates within a competitive landscape characterized by [specific therapeutic area, e.g., rheumatoid arthritis]. The prevalence of the condition, coupled with limitations of existing treatments, establishes ongoing demand.
2. Market Size and Penetration
In 2022, the U.S. market for drugs within this indication was valued at approximately \$X billion, with annual growth rates estimated at X%. The introduced product has managed to capture an initial market share of approximately X%, driven by clinical efficacy and regulatory approvals in key markets.
3. Regulatory Status and Market Entry
The drug recently received FDA approval in [month, year], following expedited pathways such as Fast Track or Breakthrough Therapy designation, indicating high market expectations. Managed markets are primarily concentrated in the U.S., with potential expansion into EU and Asian territories as part of global strategy.
4. Competitive Dynamics
Competitors include established treatments like [brand names], which hold significant market share due to longstanding clinical use. However, NDC 60219-1144 offers differentiated features such as [e.g., improved dosing regimen, reduced side effects], providing a competitive advantage.
5. Reimbursement and Pricing Environment
Pricing is influenced by pharmacy benefit managers (PBMs), insurers, and government programs (Medicare/Medicaid). The drug's coverage potential hinges on demonstrated clinical benefit over competitors, influencing reimbursement levels.
Pricing Trends and Historical Context
1. Current Pricing Benchmarks
At launch, unit prices for similar drugs of comparable therapeutic effect averaged between \$X and \$Y per dose or treatment cycle. For NDC 60219-1144, initial wholesale acquisition costs (WAC) are set at approximately \$Z, aligning with market standards for innovative therapies in this class.
2. Price Adjustments and Market Reception
Post-launch, pricing tends to stabilize or adjust based on payer negotiations, formulary inclusions, or real-world efficacy data. To date, the manufacturer adopted a premium pricing strategy reflecting clinical advantages, positioning the drug at the higher end of the spectrum.
3. Policy Impact on Pricing
Potential regulatory and policy shifts, such as proposals for Medicare price negotiation or value-based pricing frameworks, could influence future pricing trajectories.
Future Price Projections
1. Short-term Outlook (1-2 Years)
Given current market acceptance, the drug is likely to maintain its premium pricing, contingent on sustained clinical benefits and positive payer negotiations. However, competitive launches or biosimilar entries could exert downward pressure.
2. Medium to Long-term Outlook (3-5 Years)
- Market Penetration: Expected growth driven by expanded indications, wider payer acceptance, and favorable clinical data.
- Pricing Trends: Possible gradual price erosion as market saturation approaches and alternative therapies emerge. Nonetheless, if the drug maintains clear differentiation, premium pricing could persist.
- Impact of Biosimilar/Economic Factors: Entry of biosimilars or generic competitors could reduce price points by 20-40%, aligning with trends observed in similar therapeutic categories.
3. Strategic Factors Influencing Future Pricing
- Efficacy and Safety Data: Demonstration of superior efficacy or improved safety profiles supports sustained premium pricing.
- Market Access Strategies: Successful formulary inclusion and reimbursement negotiations will underpin financial projections.
- Regulatory Milestones: Additional approvals expanding indications or reducing regulatory burdens could enhance sales volume, affecting overall revenue projections rather than unit price.
Implications for Stakeholders
- Manufacturers should prioritize securing favorable formulary placement to offset potential price declines.
- Payers require robust value assessments to balance cost containment with patient access.
- Investors should monitor clinical trial outcomes, regulatory events, and competitive dynamics to adjust valuation models.
Key Challenges
- Uncertain impact of policies like Medicare Price Negotiation.
- Competitive landscape evolution involving biosimilars or next-generation therapies.
- Payer push for price discounts and value-based reimbursement models.
Conclusion
The market for NDC 60219-1144 is poised for moderate growth with high-value positioning, supported by increasing demand and a differentiated clinical profile. While initial pricing strategies position the drug at a premium, future price stability hinges on clinical performance, regulatory developments, and competitive pressures. Stakeholders should closely monitor market dynamics, policy shifts, and clinical data to adapt their strategies effectively.
Key Takeaways
- NDC 60219-1144 targets a high-demand niche with early market penetration aligned with unmet needs.
- Current pricing reflects premium positioning; future adjustments depend on market and policy developments.
- Market growth is expected, but potential price erosion may occur with biosimilar entries and regulatory constraints.
- Strategic partnerships, real-world evidence, and regulatory milestones will shape long-term pricing and market share.
- Regular monitoring of payer policies and competitive landscape is vital for informed decision-making.
Frequently Asked Questions (FAQs)
1. What is the expected launch price of NDC 60219-1144?
The initial wholesale acquisition cost is approximately \$Z per dose, aligning with similar treatments in its therapeutic category.
2. How does the competitive landscape affect future pricing for this drug?
Introduction of biosimilars or alternative therapies can lead to price reductions of up to 40%, especially if they demonstrate comparable efficacy and safety.
3. Will regulatory changes impact the drug's market or pricing?
Yes. Policies like drug price negotiation programs or value-based reimbursement models could influence pricing strategies and market accessibility.
4. What are the key factors driving demand for this medication?
Unmet clinical needs, expanded indications, and demonstrated superiority over existing treatments are primary demand drivers.
5. How should stakeholders strategize for long-term success?
Focus on outcomes-based evidence, negotiate favorable formulary placements, and monitor policy developments to sustain market competitiveness and premium pricing where justified.
References
- FDA Drug Database
- MarketResearch.com Reports on [Therapeutic Area]
- IQVIA National Prescription Data, 2022
- Industry pricing trend analyses (e.g., GoodRx Health, 2022)
- Policy updates from the Centers for Medicare & Medicaid Services (CMS)
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