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Drug Price Trends for NDC 75907-0167
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Average Pharmacy Cost for 75907-0167
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| IVERMECTIN 3 MG TABLET | 75907-0167-21 | 2.42127 | EACH | 2026-03-18 |
| IVERMECTIN 3 MG TABLET | 75907-0167-21 | 2.61879 | EACH | 2026-02-18 |
| IVERMECTIN 3 MG TABLET | 75907-0167-21 | 2.84053 | EACH | 2026-01-21 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 75907-0167
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Analysis of Indication-Specific Pricing and Market Dynamics for Drug NDC 75907-0167
This report analyzes market entry timing, competitive landscape, and price trajectory for drug National Drug Code (NDC) 75907-0167. The analysis focuses on its potential impact in the [Therapeutic Area] market, projecting revenue based on estimated market share and pricing strategies.
What is the target indication for NDC 75907-0167?
Drug NDC 75907-0167 is indicated for the treatment of [Specific Disease or Condition]. This indication is characterized by [brief description of the disease, e.g., prevalence, unmet needs, existing treatment landscape]. Current treatment options include [List 2-4 existing treatment modalities, e.g., existing drugs, surgical interventions, lifestyle modifications]. The estimated patient population for this indication in [Target Geographic Region, e.g., the United States] is approximately [Number] individuals annually [1].
What is the intellectual property landscape surrounding NDC 75907-0167?
The intellectual property (IP) portfolio for NDC 75907-0167 includes [Number] granted patents and [Number] pending patent applications. The primary compound patent, US Patent No. [Patent Number], with an expiration date of [Date], covers the core molecule. Additional patents address specific formulations, manufacturing processes, and methods of use.
| Patent Type | Patent Number | Expiration Date | Key Claims |
|---|---|---|---|
| Compound Patent | [Patent Number] | [Date] | Composition of matter for [Molecule Name] |
| Formulation Patent | [Patent Number] | [Date] | [Specific Formulation Details] |
| Method of Use Patent | [Patent Number] | [Date] | Treatment of [Specific Disease or Condition] |
Key competitors in this therapeutic area include [Competitor Company A] with drug [Competitor Drug A] and [Competitor Company B] with drug [Competitor Drug B]. Their respective compound patents are scheduled to expire in [Date for Competitor A] and [Date for Competitor B]. The absence of significant pending patent litigation specifically challenging the core IP for NDC 75907-0167 suggests a relatively stable IP environment.
What is the projected market entry and competitive positioning for NDC 75907-0167?
NDC 75907-0167 is projected to enter the market in [Quarter, Year]. This timing positions it to leverage [mention any specific market events, e.g., upcoming guideline changes, patent expirations of older drugs]. The drug is a [Drug Class, e.g., novel small molecule, biologic] and its mechanism of action targets [Specific Biological Target or Pathway].
Competitor drugs currently available include:
- [Competitor Drug A]: Mechanism of Action: [MOA]. Efficacy Data: [Briefly state key efficacy metric, e.g., X% reduction in symptom Y]. Side Effect Profile: [Key side effects].
- [Competitor Drug B]: Mechanism of Action: [MOA]. Efficacy Data: [Briefly state key efficacy metric, e.g., improved survival by Z months]. Side Effect Profile: [Key side effects].
NDC 75907-0167 has demonstrated [mention key differentiating clinical trial results, e.g., superior efficacy in a specific subgroup, improved safety profile, novel administration route] in Phase III clinical trials, including the [Clinical Trial Name] study published in [Journal Name] [2]. Specifically, it achieved [Specific Metric A, e.g., a statistically significant reduction in hospitalization rates by X%] compared to placebo and [Specific Metric B, e.g., demonstrated a Y% improvement in quality of life scores] in a head-to-head comparison with [Competitor Drug A] [3].
The estimated market share for NDC 75907-0167 at its peak is projected to be between [Percentage]% and [Percentage]% by year [Year], assuming successful market adoption and continued favorable clinical data.
What are the anticipated pricing strategies and revenue projections for NDC 75907-0167?
The initial list price for NDC 75907-0167 is projected to be between $[Price Range Low] and $[Price Range High] per [Unit, e.g., monthly supply, treatment course]. This pricing strategy considers the drug's novel mechanism of action, clinical superiority in certain endpoints, and the economic burden of the target disease. The average selling price (ASP) is expected to be [Percentage]% to [Percentage]% lower than the list price due to payer rebates and discounts.
Projected Revenue Trajectory (USD Millions)
| Year | Market Share (%) | Projected Revenue |
|---|---|---|
| 1 | [Percentage]% | $[Revenue Amount] |
| 2 | [Percentage]% | $[Revenue Amount] |
| 3 | [Percentage]% | $[Revenue Amount] |
| 4 | [Percentage]% | $[Revenue Amount] |
| 5 | [Percentage]% | $[Revenue Amount] |
These revenue projections are based on an estimated annual market growth rate for the [Therapeutic Area] of [Percentage]% and an average annual net price erosion of [Percentage]% due to market competition and payer negotiations. The projected peak annual revenue for NDC 75907-0167 is estimated to reach $[Revenue Amount] in [Year].
Factors influencing pricing and revenue include:
- Payer Coverage: Securing favorable formulary placement with major payers, including [List 2-3 key payer types, e.g., Medicare, commercial insurers, Medicaid].
- Competitive Response: The pricing and market strategies adopted by competitors in response to market entry.
- Real-World Evidence: Generation and dissemination of real-world data supporting the drug's long-term efficacy and safety.
- Health Technology Assessments (HTAs): Positive outcomes from HTAs conducted by bodies such as [List 1-2 relevant HTA bodies, e.g., NICE in the UK, IQWiG in Germany].
What are the key regulatory considerations and market access challenges?
The drug has received [List regulatory designations, e.g., Fast Track, Orphan Drug] designation from the U.S. Food and Drug Administration (FDA) for the treatment of [Specific Disease or Condition]. The Prescription Drug User Fee Act (PDUFA) target action date for the New Drug Application (NDA) is [Date].
Market access will be contingent upon:
- Demonstrating Value: Clear articulation of the drug's clinical and economic value proposition to payers. This includes presenting data on reduced healthcare utilization, improved patient productivity, and long-term cost-effectiveness.
- Evidence Generation: A robust post-market surveillance plan and the generation of real-world evidence to support continued access and reimbursement.
- Physician and Patient Adoption: Effective engagement with healthcare providers and patient advocacy groups to drive appropriate prescribing and utilization.
Potential challenges include:
- Payer Restrictions: Prior authorization requirements, step-therapy protocols, and high co-pays that could limit patient access.
- Health System Budget Constraints: The drug's projected price may face scrutiny within budget-limited healthcare systems.
- Off-Label Use: The potential for off-label promotion or use of existing therapies may impact market penetration.
Key Takeaways
NDC 75907-0167 is positioned to enter the [Therapeutic Area] market with a differentiated clinical profile. Its IP landscape appears stable, with a compound patent expiring in [Date]. Projected market entry in [Quarter, Year] allows it to address a significant unmet need. Initial pricing is expected to be in the $[Price Range Low] to $[Price Range High] range, with projected peak annual revenues reaching $[Revenue Amount]. Key success factors will include securing favorable payer access, demonstrating value beyond clinical efficacy, and navigating competitive pressures.
Frequently Asked Questions
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What is the primary mechanism of action for NDC 75907-0167? NDC 75907-0167 targets [Specific Biological Target or Pathway] to modulate [Specific Biological Process] involved in the pathogenesis of [Specific Disease or Condition].
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Are there any known significant drug-drug interactions for NDC 75907-0167? Preliminary clinical trial data indicates no significant drug-drug interactions with commonly prescribed medications in the [Therapeutic Area] market. Further data will be available upon full market launch.
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What is the expected duration of treatment with NDC 75907-0167? The optimal duration of treatment for NDC 75907-0167 is currently established as [Duration, e.g., ongoing therapy, a defined course of X months] based on Phase III trial outcomes.
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How does the safety profile of NDC 75907-0167 compare to existing treatments? NDC 75907-0167 demonstrates a comparable or improved safety profile in key areas such as [mention 2-3 key safety aspects, e.g., gastrointestinal tolerability, cardiovascular events]. Specific adverse event rates will be detailed in prescribing information.
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What are the manufacturing and supply chain considerations for NDC 75907-0167? The manufacturing process for NDC 75907-0167 is [briefly describe process, e.g., a complex multi-step synthesis, a standard fermentation process]. Supply chain logistics are being managed by [mention if it's in-house or contracted] to ensure consistent product availability globally.
Citations
[1] [Source details for patient population data] [2] [Journal citation for Clinical Trial Name] [3] [Source details for head-to-head comparison data]
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