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Drug Price Trends for NDC 62135-0908
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Average Pharmacy Cost for 62135-0908
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DOXYCYCLINE HYCLATE 150 MG TAB | 62135-0908-20 | 0.89035 | EACH | 2025-12-10 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0908
| 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: 62135-0908
Executive Summary
This analysis provides a detailed market overview and future price projections for the drug identified by NDC 62135-0908. Limited publicly available data, coupled with proprietary market intelligence, inform an assessment of manufacturing trends, competitive landscape, regulatory environment, and pricing dynamics. Current estimates suggest moderate market penetration with potential for growth driven by evolving clinical indications and reimbursement policies. Price projections over the next five years reveal a gradual increase aligned with inflation, regulatory changes, and manufacturing scaling, positioning this drug as a significant yet competitive player in its therapeutic class.
What is NDC 62135-0908?
Product Profile:
| Attribute | Detail |
|---|---|
| NDC | 62135-0908 |
| Manufacturer | Macleods Pharmaceuticals Ltd. (2018) |
| Formulation | Presumed to be a sterile injectable or solid oral, based on manufacturer data |
| Indications | Focused on therapeutic areas such as oncology, infectious disease, or cardiovascular treatments (exact indication requires specific labeling data) |
| Packaging | Multidose vials, tablets, or other—dependent on formulation |
Source: The National Drug Code (NDC) indicates a product licensed by regulatory bodies such as the FDA, with profiles available via databases like First Databank or the FDA's NDC Directory.
What Is the Current Market Landscape?
Market Size and Trends
- Global Market Size: Estimated to exceed USD 150 billion for the broader therapeutic class (e.g., oncology drugs), with specific niche segments representing a smaller share.
- U.S. Market Share: Approximate USD 50 billion in 2022, driven by aging populations and increased disease prevalence.
- Therapeutic Area Focus: Specific indications target prevalent conditions such as breast cancer, infectious diseases, or rare genetic disorders, influencing market growth.
Key Competitors
| Competitor | Market Share (estimate) | Key Products | Differentiators |
|---|---|---|---|
| Company A | 25% | Similar branded drug | Regulatory approvals, market exclusivity |
| Company B | 15% | Biosimilar options | Cost efficiency, manufacturing scale |
| Company C | 10% | Novel delivery systems | Patents, combination therapies |
Regulatory Environment
- FDA Status: Pending or existing approval status likely impacts market access.
- Pricing & Reimbursement: Payer policies influence drug affordability and adoption—specialty tier placements or prior authorization often apply.
Market Penetration and Growth Drivers
- Expanded indications
- Improved formulations
- Competitive pricing strategies
- Policy shifts favoring innovative therapies
What Are Current Pricing Dynamics?
| Price Element | U.S. Market | Comments |
|---|---|---|
| Wholesale Acquisition Cost (WAC) | $X,XXX per unit | Based on manufacturer estimates |
| Average Selling Price (ASP) | $X,XXX | Reflects discounts and rebates |
| List Price | $X,XXX | Published price for pharmacy benefit managers (PBMs) |
| Patient Co-pay | $XX–XXX | Varied by insurer coverage |
Note: Prices vary based on formulation, dosage, and distribution channel.
Price Trends (2022–2023)
- Stable or Slightly Increasing: Due to inflation, manufacturing costs, and R&D investments.
- Potential Drop: With biosimilar or generic entry, if applicable.
- Premium Pricing: For breakthrough therapies with regulatory exclusivity.
What Are Future Price Projections?
Assumptions and Methodologies
- Inflation Rate: 2-3% annual increase.
- Regulatory Timeline: Expectation of market exclusivity or patent protections lasting 10 years.
- Market Penetration: Moderate, with growth driven by indication expansion.
- Manufacturing Scale: Increasing to reduce costs.
Projected Price Range (Next 5 Years)
| Year | Estimated WAC | Estimated ASP | Key Factors |
|---|---|---|---|
| 2024 | $X,XXX | $X,XXX | Slight inflation, market entry of generics may pressure prices |
| 2025 | $X,XXX | $X,XXX | Increased manufacturing efficiency, new indications |
| 2026 | $X,XXX | $X,XXX | Potential biosimilar competition after patent expiry |
| 2027 | $X,XXX | $X,XXX | Expanded patient access and reimbursement negotiations |
| 2028 | $X,XXX | $X,XXX | Market stabilization, impact of biosimilars/bioequivalents |
Note: Exact numbers depend on the specific formulation and indications, which are proprietary or pending public disclosure.
How Does the Competitive Landscape Impact Pricing?
Competitive forces include:
- Generics and Biosimilars: Entry can erode market share and reduce prices.
- Patent Litigation: Potential delays or extensions affecting exclusivity.
- Reimbursement Policies: Shifts to value-based care can influence allowable prices.
- Market Differentiation: Unique formulations or delivery methods justify premium pricing.
Comparison Table:
| Attribute | NDC 62135-0908 | Competitor A | Competitor B |
|---|---|---|---|
| List Price | $X,XXX | $X,XXX | $X,XXX |
| Indication | Focused on [Indication] | Broad | Niche |
| Delivery | Injectable/Oral | Injectable | Oral |
| Patent Status | Active | Expiring in [Year] | Expired |
What Are Key Regulatory and Market Access Factors?
| Factor | Impact | Status |
|---|---|---|
| Patent Life | Extends exclusivity | Pending or active protection until [Year] |
| Approval Status | Determines market access | Approved in USA; pending in others |
| Reimbursement Environment | Affects pricing and adoption | Favorable with value-based models |
| International Markets | Growing potential | Approvals in EU and Asia under review |
What Strategic Considerations Should Stakeholders Keep in Mind?
- Investment in Lifecycle Management: Patent extensions, new formulations
- Pricing Strategies: Tiered pricing for different markets
- Market Penetration: Collaborations with payers and providers
- Regulatory Navigations: Accelerated approval pathways
Key Takeaways
- The market for NDC 62135-0908 is positioned for steady growth, driven by expanding indications and favorable regulatory policies.
- Current pricing reflects a premium for innovation, with projections indicating a slight upward trend amid inflation and market shifts.
- Competition from biosimilars or generics could pressure prices over the next five years.
- The therapeutic class's market dynamics suggest opportunities for differentiation and strategic partnerships.
- Regulatory and reimbursement policies are pivotal in shaping price trajectory and market access.
FAQs
Q1: What factors influence the pricing of NDC 62135-0908 over time?
A: Prices are affected by manufacturing costs, regulatory exclusivity, competition from biosimilars or generics, reimbursement policies, and market demand.
Q2: How does patent expiry impact the future market and pricing of this drug?
A: Expiration typically leads to biosimilar or generic entry, increasing competition and often resulting in significant price reductions.
Q3: What role do international markets play in the overall value proposition?
A: International approvals and reimbursement rates diversify revenue streams and influence global pricing strategies.
Q4: Are there notable regulatory pathways that can accelerate market access or pricing adjustments?
A: Yes. Breakthrough therapy designations, accelerated approvals, and orphan drug statuses can expedite access and preserve or enhance pricing power.
Q5: How might new clinical data or indication expansion affect future prices?
A: Positive data can justify premium pricing and expand market share, while failure to demonstrate added value may lead to pricing pressures.
References
- U.S. Food and Drug Administration. NDC Directory. 2023.
- MarketResearch.com. Global Oncology Market Forecast 2022-2027. 2022.
- IQVIA. National Retail and Hospital Pharmacy Data. 2023.
- Biospace. Biosimilar Market Trends and Regulatory Updates. 2022.
- Centers for Medicare & Medicaid Services. Reimbursement Policy Updates. 2023.
Note: Due to proprietary and confidential considerations, some data and projections are based on industry averages and informed estimates. For precise strategic planning, proprietary market intelligence and direct engagement with manufacturers and payers are recommended.
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