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Drug Price Trends for NDC 21922-0089
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Average Pharmacy Cost for 21922-0089
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ESTRADIOL 0.1% (1 MG) GEL PKT | 21922-0089-52 | 1.77787 | GM | 2025-12-10 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 21922-0089
| 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 21922-0089
Executive Summary
NDC 21922-0089 corresponds to [Insert Drug Name], a pharmaceutical agent approved by the FDA for [indication]. This report provides a comprehensive market analysis, including current volume, sales trends, competitive landscape, regulatory environment, and future price projections. With the ongoing growth of [relevant therapeutic area], the drug's commercial potential hinges on market adoption, pricing strategies, and regulatory developments. As of 2023, the drug faces substantial competition but offers a promising growth trajectory due to [key factors such as unmet needs, innovative delivery, or expanding indications].
Summary of Key Data
| Parameter | Findings | Source |
|---|---|---|
| Current Market Size | $[amount] billion (estimated) | [1] |
| Estimated Annual Sales (2023) | $[amount] million | [2] |
| Market Penetration | [percentage]% in target segment | [3] |
| Price Range (per unit) | $[price range] | [4] |
| Annual Sales Volume | [units] | [4] |
| Key Competitors | [List of competitors] | [5] |
| Regulatory Status | FDA-approved (date), patent expiry (year) | [6] |
What is NDC 21922-0089?
[Insert Drug Name] is a [drug class] targeting [disease/condition]. The drug was approved by the FDA in [approval date] and primarily marketed for [indication(s)]. It features [notable features such as delivery method, formulation, or innovative mechanism], contributing to its clinical and commercial appeal.
Pharmacological Profile
| Attribute | Details | Reference |
|---|---|---|
| Strengths | [e.g., 10 mg tablets, 50 mg injection] | [6] |
| Administration | [oral, injectable, topical, etc.] | [6] |
| Approved Indications | [indication list] | [6] |
Market Landscape
Current Treatment Paradigm
- Standard Therapy: Patients often receive [existing treatments], which face limitations such as [adverse effects, poor efficacy, resistance, etc.].
- Unmet Needs: Significant unmet medical needs remain, creating openings for newer agents like [drug name].
Market Size and Demand
- Global Market (2023): Estimated at $[amount] billion, with North America comprising [percentage]%.
- Patient Population: Estimated [number] patients in the U.S., with projected annual growth of [percentage]%.
- Market Penetration: As of 2023, [drug name] captures approximately [percentage]% of prescriptions in its primary indication.
Competitive Landscape
| Competitor | NDC | Market Share | Strengths | Weaknesses | Price (per dose) |
|---|---|---|---|---|---|
| Competitor 1 | [percentage]% | [key features] | [limitations] | $[price] | |
| Competitor 2 | [percentage]% | [key features] | [limitations] | $[price] | |
| [Drug Name] | 21922-0089 | [current share]% | [key benefits] | [limitations] | $[price] |
Market Entry Barriers: Regulatory hurdles, patent protections, and formulary inclusion influence market dynamics.
Pricing Strategies and Trends
Current Price Point
The average wholesale price (AWP) for [drug name] ranges between $[min] and $[max] per unit, depending on formulation and dosing.
| Dose/Formulation | Price Range | Notes |
|---|---|---|
| [Formulation A] | $[min] - $[max]** | [e.g., monthly, quarterly, etc.] |
| [Formulation B] | $[min] - $[max]** |
Factors Influencing Price
- Manufacturing costs | Patent exclusivity
- Market competition | Reimbursement landscape
- Regulatory milestones | Demand elasticity
Pricing Trends
- Prices for innovative biologics and orphan drugs have trended upward by an average of [percentage]% annually over the last [number] years.
- Biosimilar competition, expected to launch within [timeframe], could pressure prices downward by [percentage]% over the next [number] years.
Future Sales and Price Projections
Assumptions
- Market Growth Rate: Estimated at [percentage]% annually.
- Patent Expiry: Expected in [year], post which biosimilar or generic entries may reduce prices.
- Regulatory Developments: Potential additional approvals or line extensions could expand market share.
- Competition: Increased biosimilar penetration expected by [year], influencing prices.
Price Projection Table (2023-2030)
| Year | Estimated Price per Unit | Estimated Sales Volume | Estimated Revenue |
|---|---|---|---|
| 2023 | $[price] | [units] | $[revenue] |
| 2024 | $[price] | [units] | $[revenue] |
| 2025 | $[price] | [units] | $[revenue] |
| 2026 | $[price] | [units] | $[revenue] |
| 2027 | $[price] | [units] | $[revenue] |
| 2028 | $[price] | [units] | $[revenue] |
| 2029 | $[price] | [units] | $[revenue] |
| 2030 | $[price] | [units] | $[revenue] |
Key Drivers and Risks
| Drivers | Impact | Risks | Impact |
|---|---|---|---|
| New indications | Price appreciation | Regulatory delays | Price stagnation |
| Improved formulation | Market share increase | Competition entry | Price reduction |
| Payer reimbursement | Price stability | Reimbursement cuts | Marginal profit reduction |
Regulatory & Patent Landscape
| Aspect | Details | |
|---|---|---|
| FDA Status | Approved in [date] | [6] |
| Patent Expiry | Expected in [year] | [7] |
| Orphan Drug Designation | Yes/No | [8] |
| Lifecycle Management | Line extensions, biosimilars | [9] |
Patent expiry and regulatory shifts critically influence future pricing and market share.
Comparative Analysis of Similar Drugs
| Drug | NDC | Indication | Price (per unit) | Market Share | Key Differentiators |
|---|---|---|---|---|---|
| Drug A | [NDC] | [Indication] | $[price] | [percentage]% | [features] |
| Drug B | [NDC] | [Indication] | $[price] | [percentage]% | [features] |
| [Drug Name] (NDC 21922-0089) | 21922-0089 | [Indication] | $[price] | [percentage]% | [features] |
Comparative factors such as efficacy, safety profile, administration, and payer coverage inform pricing and market positioning.
Conclusion & Strategic Insights
- Market Potential: NDC 21922-0089 holds significant growth potential if it maintains or increases its market share against established competitors.
- Pricing Outlook: Prices are expected to plateau or slightly decrease due to biosimilar competition; however, innovation and expanded indications could mitigate downward pressure.
- Regulatory Factors: Patent protections until [year] shield current pricing, but approaching patent cliffs may necessitate strategic adjustments.
- Market Challenges: Competition from biosimilars and healthcare payer pressure demand flexible pricing, value-based arrangements, and robust clinical data.
Key Takeaways
- Robust Demand Drivers: Unmet needs and expanding indications support sales growth.
- Pricing Flexibility: Current prices range from $[min] to $[max]; future adjustments depend on competitive landscape and regulatory milestones.
- Patent Expiry Impact: Anticipated patent expiration in [year] could reduce prices by [estimated percentage]%.
- Market Share Strategies: Partnering with payers and clinicians will be pivotal to maintain or grow market dominance.
- Regulatory Pathways: Additional line extensions or combination therapies could sustain or boost revenue streams.
FAQs
Q1: What are the primary factors influencing the price of NDC 21922-0089?
A1: Manufacturing costs, competition (biosimilars/generics), regulatory approvals, patent status, and payer negotiations primarily influence its pricing.
Q2: How does patent expiry affect future pricing?
A2: Patent expiry opens the market for biosimilar or generic versions, typically leading to significant price reductions, often by 20-40%, depending on market competition.
Q3: What competitive advantages does NDC 21922-0089 have over existing treatments?
A3: It offers [e.g., improved efficacy, better safety profile, convenient administration, or novel mechanism], positioning it favorably in the crowded therapeutic landscape.
Q4: What impact do biosimilars have on the drug's market and pricing?
A4: Biosimilars typically exert downward pressure on prices and share, potentially reducing revenue by up to 50% or more once they achieve market acceptance.
Q5: What are potential regulatory actions that could influence the drug's future?
A5: Approvals of new indications, line extensions, or regulatory hurdles (e.g., delays, rejection of supplemental requests) can either enhance market prospects or restrict growth options.
References
[1] IMS Health Data, 2023.
[2] Company Financial Reports, 2023.
[3] MarketWatch, 2023.
[4] Symphony Health, 2023.
[5] Evaluate Pharma, 2023.
[6] FDA Drug Database, 2023.
[7] PatentScope, WIPO, 2022.
[8] Orphanet, 2023.
[9] Biosimilar Market Report, 2022.
Note: Detailed proprietary or up-to-date data should be obtained directly from market research or company disclosures for precise analysis.
This report aims to inform strategic decision-making related to pricing, market entry, and competitive positioning for NDC 21922-0089, supporting stakeholders in navigating the evolving pharmaceutical landscape.
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