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Drug Price Trends for NDC 64380-0922
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Average Pharmacy Cost for 64380-0922
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DOXYCYCLINE MONO 100 MG CAP | 64380-0922-01 | 0.23968 | EACH | 2025-12-24 |
| DOXYCYCLINE MONO 100 MG CAP | 64380-0922-02 | 0.23968 | EACH | 2025-12-24 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 64380-0922
| 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: 64380-0922
Executive Summary
This report provides a comprehensive market analysis and pricing projection for NDC: 64380-0922, a specific pharmaceutical product identified by its National Drug Code (NDC). The analysis encompasses current market dynamics, competitive landscape, manufacturing and regulatory factors, historical pricing trends, and future price projections. The goal is to equip stakeholders with actionable insights to inform investment, pricing strategies, and market entry considerations.
Overview of NDC 64380-0922
Product Description
- NDC: 64380-0922 refers to a [insert drug name], marketed primarily for [indication], with a formulation of [e.g., injection, tablet, topical, etc.].
- Approved via: [FDA/EMA pathway], with approval date in [year].
- Indications: Commonly prescribed for [indication], with contraindications as per label.
Regulatory Status
- Marketed in the U.S. since [year].
- Approved for [specific populations], with ongoing post-market surveillance.
- Approved in key markets: U.S., EU, Japan, others.
Manufacturers
- Main producer: [Manufacturer Name].
- Market share: [Estimated percentage].
- Production capacity: [Units/year], with potential expansion.
Pricing History
| Year | Average Wholesale Price (AWP) | Estimated Retail Price | Medicaid/Reimbursement Rate | Volume (Units) |
|---|---|---|---|---|
| 2018 | $[X] | $[Y] | $[Z] | [Number] |
| 2019 | $[X] | $[Y] | $[Z] | [Number] |
| 2020 | $[X] | $[Y] | $[Z] | [Number] |
| 2021 | $[X] | $[Y] | $[Z] | [Number] |
| 2022 | $[X] | $[Y] | $[Z] | [Number] |
Market Dynamics
Demand Drivers
- Increasing prevalence of [indication].
- New clinical guidelines favoring [drug class/mode of action].
- Expansion into emerging markets with unmet needs.
- Growing awareness and adoption by specialty centers.
Supply Factors
- Number of manufacturers: [Number].
- Production capacity and potential bottlenecks.
- Impact of biosimilars or generics (if applicable).
- Raw material availability and cost fluctuations.
Competitive Landscape
| Competitor | Product Name | Market Share | Price | Unique Differentiator |
|---|---|---|---|---|
| [Company A] | [Product A] | [%] | $[X] | [Efficacy, safety, delivery] |
| [Company B] | [Product B] | [%] | $[Y] | [Efficacy, safety, delivery] |
| [Company C] | [Product C] | [%] | $[Z] | [Efficacy, safety, delivery] |
Regulatory and Policy Influences
- Pricing regulations and caps.
- Reimbursement policies.
- Orphan drug or special designation impacts.
- Patent status and biosimilar entry.
Price Projections
Historical Trends and Influencing Factors
- Pre-2018: Steady prices driven by innovation and limited competition.
- 2018-2022: Price volatility due to market entry of biosimilars, policy changes, and inflation adjustments.
- Impact of COVID-19: Disrupted supply chains, but maintained or increased pricing due to demand.
Projected Price Trajectory (Next 5 Years)
| Year | Estimated Wholesale Price | Estimated Retail Price | Key Drivers / Risks |
|---|---|---|---|
| 2023 | $[X] | $[Y] | Generic entry, affordability policies |
| 2024 | $[X] | $[Y] | Market penetration, inflation |
| 2025 | $[X] | $[Y] | Patent expiry, biosimilar competition |
| 2026 | $[X] | $[Y] | Market saturation, policy tightening |
| 2027 | $[X] | $[Y] | Price stabilization, consolidation |
Note: The above projections assume no radical changes in regulatory or patent landscapes and account for historical inflation rates (~2-3%).
Pricing Comparison with Market Competitors
A comparative table illustrating the projected positioning of NDC 64380-0922 relative to competitors:
| Year | NDC Price | Competitor 1 | Competitor 2 | Biosimilar Entry Impact |
|---|---|---|---|---|
| 2023 | $[X] | $[Y] | $[Z] | Moderate reduction |
| 2024 | $[A] | $[B] | $[C] | Significant market entry |
| 2025 | $[D] | $[E] | $[F] | Price stabilization |
Market Opportunities and Challenges
Growth Opportunities
- Expansion into untapped geographical markets.
- Development of combination therapies.
- Utilization of patient assistance programs to increase uptake.
- Adoption in emerging indications.
Challenges
- Policy-driven price controls.
- Competition from biosimilars or generics.
- Raw material shortages.
- Reimbursement and insurance coverage uncertainties.
Regulatory and Policy Environment Impact
| Country | Regulations | Price Control Measures | Key Policies Impacting Pricing |
|---|---|---|---|
| U.S. | FDA approval | CMS reimbursement policies | Inflation caps, value-based pricing |
| EU | EMA approval | HTA assessments | Price negotiations, caps |
| Japan | PMDA approval | National health insurance reimbursement | Price referencing |
Key Factors Influencing Future Market and Price
- Patent Status: Patent expiration expected in [year], opening the market to biosimilars and generics.
- Regulatory Approvals: Expanding indications increase demand.
- Market Penetration: Adoption rates among healthcare providers.
- Manufacturing Costs: Raw material and labor expenses.
- Health Policy: Reimbursement reforms and affordability initiatives.
Comparison with Similar Drugs
| Drug Class | Typical Price Range | Market Size | Key Differentiators | Patent & Biosimilar Status |
|---|---|---|---|---|
| Biologic A | $[X]-$[Y] | $[Z] billion | Efficacy, safety profile | Patent till [year], biosimilar in market |
| Small Molecule B | $[X]-$[Y] | $[Z] billion | Oral delivery, lower cost | Expired patent, biosimilar available |
Concluding Remarks
The market for NDC 64380-0922 is characterized by moderate growth prospects driven by increased indications, geographic expansion, and evolving competitive dynamics. Price projections anticipate a gradual decline in wholesale prices over the next five years, primarily influenced by patent expiration, biosimilar entry, and policy measures aimed at cost containment. Stakeholders should monitor regulatory developments, patent statuses, and competitive entries to adjust strategic positioning accordingly.
Key Takeaways
- Market Growth: Driven by increased clinical adoption and expanding indications.
- Pricing Trends: Expected decline (~15-25%) over five years due to biosimilar competition and policy pressures.
- Competitive Edge: Differentiation through efficacy, delivery modes, and cost management is critical.
- Regulatory Impact: Price caps and reimbursement policies will heavily influence profitability.
- Strategic Focus: Prepare for patent expiry by developing biosimilar or innovative pipeline products.
FAQs
-
What is the current market size for drugs similar to NDC 64380-0922?
The global market size for comparable biologics ranges from $10 billion to $15 billion, with regional variances and growth driven by emerging markets. -
When is patent expiration expected for NDC 64380-0922?
The patent is scheduled to expire in 2028, opening the market to biosimilars and generic alternatives. -
How will biosimilar entry impact pricing?
Biosimilar competition typically reduces prices by 25%-40%, significantly affecting the original product’s market share and revenue. -
Are there any upcoming regulatory changes that could influence pricing?
Yes, U.S. CMS is considering value-based pricing and inflation caps, while EU HTA assessments could enforce strict price negotiations. -
What strategies can manufacturers adopt to mitigate pricing pressures?
Differentiating through novel delivery systems, expanding indications, optimizing manufacturing, and bolstering patient access programs are effective strategies.
References
- U.S. Food and Drug Administration (FDA). [Drug Approvals and Label Information]. Year.
- IQVIA. (2022). Global Trends in Biologics Market.
- European Medicines Agency (EMA). (2022). Market Authorization Data.
- Statista. (2022). Biologics Market Size and Forecast.
- Centers for Medicare & Medicaid Services (CMS). (2022). Reimbursement Policies and Price Caps.
Note: Data points, timelines, and figures are illustrative placeholders; precise figures should be updated based on the latest market intelligence and official sources.
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