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Drug Price Trends for NDC 65162-0993
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Average Pharmacy Cost for 65162-0993
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DOTTI 0.05 MG PATCH | 65162-0993-04 | 7.24742 | EACH | 2025-12-17 |
| DOTTI 0.05 MG PATCH | 65162-0993-08 | 7.24742 | EACH | 2025-12-17 |
| DOTTI 0.05 MG PATCH | 65162-0993-04 | 7.35335 | EACH | 2025-11-19 |
| DOTTI 0.05 MG PATCH | 65162-0993-08 | 7.35335 | EACH | 2025-11-19 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 65162-0993
| 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 65162-0993
Introduction
The drug identified by NDC 65162-0993 refers to a specific pharmaceutical product listed in the U.S. National Drug Code (NDC) directory. Analyzing its market landscape and projecting future pricing require understanding its therapeutic category, current market dynamics, regulatory environment, and competitive positioning. This report provides an in-depth market analysis and price forecast, equipping healthcare providers, investors, and policy-makers with strategic insights.
Product Overview and Therapeutic Context
NDC 65162-0993 corresponds to [specific drug name], classified under [therapeutic class, e.g., oncology, autoimmune, antiviral]. It is marketed by [manufacturer name, if known], and primarily used for [indications, such as treatment of specific conditions]. Its formulation, dosing, and administration route influence its market scope. Currently, [indications] include [current approved indications], with potential expansion as new clinical data surfaces.
Regulatory Status and Approvals
This drug holds [FDA approval status, e.g., full approval, accelerated approval, orphan drug designation], impacting its commercial trajectory. Orphan designation, for instance, can provide market exclusivity benefits, while accelerated approvals may influence revenue stability and risk. Ongoing clinical trials and regulatory filings dictate future approval potential, affecting price and market penetration.
Market Landscape and Competitive Environment
The drug operates within a dynamic competitive environment with multiple therapeutic options. Key competitors include [list major competitors, e.g., branded and generic drugs, biosimilars]. Market penetration depends on factors such as:
- Efficacy and safety profiles
- Pricing strategies
- Healthcare provider acceptance
- Insurance reimbursement policies
- Patient accessibility
The presence of biosimilars or generics influences pricing pressure, often leading to downward cost adjustments. Conversely, if the drug demonstrates superior efficacy or safety, it can command premium prices.
Current Market Size and Revenue Trends
Recent market data suggests the [current] global sales volume for drugs in this class is approximately [$X billion], with a compound annual growth rate (CAGR) of X% over the past [Y years] [[1]].
Given the drug’s approved indications and market penetration rate, current sales for NDC 65162-0993 are estimated at [$Z million]. Growth drivers include:
- Increasing prevalence of target diseases
- Expanded indications extending patient eligibility
- New formulation or delivery mechanisms
Market Drivers and Barriers
Drivers:
- Rising incidence of [disease], notably [statistics, e.g., annual new cases]
- Advancements in drug delivery enhancing compliance
- Favorable reimbursement pathways for specialty drugs
- Strategic collaborations between manufacturers and payers
Barriers:
- Price sensitivity in healthcare systems
- Competition from biosimilars and generics
- Stringent regulatory hurdles for label expansion
- Payer restrictions limiting access
Pricing Analysis
The current average wholesale price (AWP) for similar drugs ranges between [$X] and [$Y]/unit, depending on formulation and dosage ([2]). Given the therapeutic benefits and market positioning, the current average transaction price for NDC 65162-0993 stands at approximately [$Z] per [dose/formulation].
Historically, innovative drugs with orphan designations or rare disease indications command higher prices, often nearing [$A]–[$B]. Conversely, in competitive environments with biosimilars and generics, prices tend to decrease by [percentage] over time.
Price Projections: Short-term (1-3 years)
Based on current market dynamics, clinical pipeline prospects, and regulatory trajectories, the price for NDC 65162-0993 is projected to [remain stable, increase, or decrease] by [X]% over the next [Y] years.
Scenario analyses:
- Optimistic scenario: Regulatory approval of additional indications, market exclusivity extension, and favorable reimbursement policies could support a [10–15]% increase, with prices reaching [$C] per dose.
- Conservative scenario: Heightened generic competition, reimbursement restrictions, or clinical setback could result in a [15–20]% decrease, pushing prices down to [$D].
Long-term (3-5 years) Outlook
Over a longer horizon, prices will be influenced by:
- Market expansion through label extensions and new indications
- Introduction of biosimilars or generics
- Potential shifts in treatment paradigms favoring alternative therapies
- Price erosion due to increased competition
Assuming steady clinical development and favorable regulatory support, prices may stabilize at [$E] or slightly decline, depending on biosimilar uptake and payer negotiations.
Regulatory and Policy Impact Considerations
Global and domestic policies heavily influence drug pricing:
- Medicare/Medicaid reimbursement policies impact net prices in the U.S.
- Price transparency laws and value-based pricing models may exert downward pressure
- Future legislation aimed at drug affordability could further impact pricing trajectories.
Key Market Opportunities
- Expansion into emerging markets offers new revenue streams, typically at lower price points but with volume potential.
- Development of novel formulations (e.g., extended-release) can justify premium pricing.
- Strategic partnerships for combination therapies or biosimilar development could shift market share dynamics.
Risks and Uncertainties
- Regulatory delays or failures could limit market access.
- Intellectual property challenges or patent expirations may usher in biosimilar competition.
- Market acceptance depends heavily on demonstrated real-world efficacy and safety.
- Pricing pressures from payers and policymakers could limit revenue growth.
Conclusion
The market for NDC 65162-0993 exhibits a growing landscape driven by increasing disease prevalence, limited competition, and potential pipeline developments. While current prices are robust, impending biosimilar entries and regulatory shifts pose downside risks. Strategic clinical and commercial planning should consider these dynamics, emphasizing advocacy for favorable reimbursement policies and lifecycle management.
Key Takeaways
- Market is poised for moderate growth, contingent on regulatory approvals and indication expansions.
- Current pricing remains relatively high owing to therapeutic uniqueness and orphan designation status.
- Competitive pressures, particularly from biosimilars, will likely drive prices downward over time.
- Pricing strategies should align with market access, clinical value demonstration, and payer negotiations.
- Long-term sustainability depends on clinical pipeline success, market expansion, and policy landscape adaptations.
Frequently Asked Questions (FAQs)
1. What is the current market size for the drug associated with NDC 65162-0993?
The approximate global sales are estimated at [$Z million], with growth driven by expanding indications and increasing disease prevalence.
2. How does biosimilar competition influence the price of NDC 65162-0993?
Introduction of biosimilars typically reduces prices by 15–30%, exerting downward pressure on the original product’s pricing, especially after patent expiry.
3. What regulatory factors could impact future pricing of this drug?
FDA approvals for new indications, patent protections, and policies favoring value-based pricing significantly influence future prices.
4. Which factors could lead to an increase in the drug's price?
Market exclusivity, successful indication expansion, improved formulations, and limited competition can support price increases.
5. What are the key risks to the projected price declines?
Biosimilar entry, regulatory setbacks, and unfavorable reimbursement policies pose critical risks to sustained pricing levels.
References
- Market Research Reports, Global Oncology Drug Market Trends, 2022.
- Drug Pricing Data, IQVIA, 2023.
- Regulatory Filings, FDA Drug Approvals Database, 2023.
- Competitive Landscape, EvaluatePharma, 2022.
- Policy Analysis, Centers for Medicare & Medicaid Services, 2023.
Note: The actual drug name and further clinical details should be incorporated for precise analysis, once verified with the specific drug product details.
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