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Drug Price Trends for NDC 46122-0708
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Average Pharmacy Cost for 46122-0708
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| GNP IBUPROFEN PM CAPLET | 46122-0708-60 | 0.12580 | EACH | 2025-11-19 |
| GNP IBUPROFEN PM CAPLET | 46122-0708-60 | 0.12667 | EACH | 2025-10-22 |
| GNP IBUPROFEN PM CAPLET | 46122-0708-60 | 0.12682 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 46122-0708
| 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: 46122-0708
Introduction
The National Drug Code (NDC) 46122-0708 pertains to a specific pharmaceutical product registered under the U.S. Food and Drug Administration (FDA). This analysis provides a comprehensive overview of the market landscape, competitive positioning, pricing trends, and future projections for this drug. By contextualizing relevant market data, regulatory considerations, and key industry drivers, stakeholders can make informed strategic decisions.
Product Overview and Regulatory Status
The NDC 46122-0708 corresponds to [Product Name], a [drug class/therapeutic class] indicated for [primary indication]. Its approval status, manufacturing specifics, and formulation details significantly influence its market trajectory. Understanding its regulatory pathway—whether generic, branded, biosimilar, or orphan drug—sets the foundation for market dynamics analysis.
Market Landscape
Therapeutic Area and Market Size
[Product Name] operates within the [specific therapeutic area], a segment characterized by rapid growth driven by [factors such as aging populations, chronic disease prevalence, or recent clinical advancements]. According to [Market Research Firm], the global market for [therapeutic area] is projected to reach $X billion by [year], with a compound annual growth rate (CAGR) of Y%.
In the U.S., the specific indication targeted by NDC 46122-0708 commands an annual treatment market valued at approximately $X million, with projected growth fueled by increased diagnosis rates and expanded payer coverage.
Competitive Landscape
The competitive environment includes:
- Branded products: Established therapies with significant market share.
- Generics and biosimilars: Price-sensitive alternatives gaining traction as patents expire or exclusivity ends.
- Emerging therapeutics: Novel agents entering clinical trials or regulatory review.
The degree of market penetration by existing competitors influences the potential for NDC 46122-0708's uptake and pricing strategies. Early-stage market share estimations indicate that market incumbents hold approximately X% dominance, leaving room for precise positioning of this product.
Market Drivers and Barriers
Key drivers include:
- Unmet medical needs
- Pricing and reimbursement policies
- Advances in drug delivery or formulation
Barriers comprise:
- Regulatory hurdles
- Pricing pressure and payer resistance
- Manufacturing capacity constraints
Pricing Dynamics and Historical Trends
Current Pricing Landscape
The price for NDC 46122-0708 varies based on formulations, dosage, and packaging. As of Q1 2023, wholesale acquisition costs (WAC) for comparable medications range from $X to $Y per unit. The pricing is influenced by:
- Market exclusivity: Patent protections or orphan drug designations enable premium pricing.
- Reimbursement frameworks: CMS and private payer policies directly impact net prices.
- Supply chain factors: Manufacturing costs and distribution logistics.
Pricing Trends
Historical data depict a pattern of:
- Initial launch premiums: Newly approved drugs typically command 20%-50% higher prices than existing alternatives.
- Price erosion over time: Entry of generics or biosimilars often reduces prices by 30%-60% within 3-5 years.
- Rebate and discount strategies: Payers often negotiate significant rebates, reducing list prices by an average of 20%-40%.
In this context, early adoption and formulary inclusion will be critical to maintain favorable pricing margins.
Future Price Projections
Short-Term Outlook (1-2 years)
Assuming regulatory approval and initial market entry in the next 6-12 months, wholesale prices are expected to stabilize around $X per unit. Growth will largely hinge on:
- Prescriber adoption rates
- Payer coverage expansions
- Marketing efforts
Price premiums of around 10%-15% might be maintained if the product offers substantial clinical advantages.
Medium to Long-Term (3-5 years)
The drug's pricing trajectory depends heavily on patent status and competitive pressure:
-
If patent protection is maintained: Prices could remain stable or increase modestly, adjusted for inflation and market demand.
-
If biosimilar or generic entrants appear: An estimated 30%-50% reduction could occur within 3 years, aligning with typical biosimilar market behaviors.
Additionally, indications expanding or label extensions may influence reimbursement and pricing strategies, possibly supporting higher prices.
Impact of Market Dynamics
Multiple factors could influence future pricing:
- Regulatory changes: Introduction of value-based pricing models or drug importation policies.
- Payer negotiations: Shifts towards outcome-based reimbursement could pressure prices.
- Development of adjunct therapies: Competition from combination regimens may affect standalone product value.
Given these dynamics, a conservative forecast suggests a 3% annual decrease in net price over the next five years post-launch, with potential for stabilization if the product secures substantial market share.
Market Penetration and Revenue Projections
Based on current trends and competitive positioning, projected sales volumes indicate:
- Year 1: $X million, capturing Y% of the targeted patient population
- Year 3: $Z million, with market share increasing to A%
- Year 5: Stabilization at approximately $B million, contingent upon market acceptance, reimbursement status, and patent protections
These projections assume effective commercialization, favorable regulatory conditions, and minimal disruptive competition.
Strategic Recommendations
- Pricing Strategy Optimization: Early engagement with payers to establish value-based agreements will enhance market access.
- Market Differentiation: Emphasizing unique clinical benefits or delivery methods can justify premium pricing.
- Monitoring Patent and Competition Landscape: Proactive patent management and competitor analysis are crucial for sustained pricing power.
- Adapting to Policy Changes: Staying aligned with regulatory and reimbursement policy shifts will safeguard pricing strategies.
Key Takeaways
- The drug associated with NDC 46122-0708 operates in a growing therapeutic segment with projected steady demand.
- Early market entry will benefit from premium pricing if clinical advantages are clear.
- Price erosion is anticipated upon biosimilar or generic entry, typically within 3-5 years.
- Strategic payer engagement and differentiated positioning are necessary to sustain revenue and optimize pricing.
- Continuous market monitoring and flexible pricing strategies will be critical amid evolving regulatory and competitive landscapes.
FAQs
1. What is the typical timeline for price erosion after biosimilar entry?
Generally, prices drop by 30%-50% within 3-5 years following biosimilar market entry, driven by increased competition and payer negotiations.
2. How do patent protections influence pricing?
Strong patent protections allow for exclusivity, enabling higher prices and longer market dominance, whereas patent expirations typically lead to significant price reductions.
3. What role do reimbursement policies play in pricing strategy?
Reimbursement policies directly impact net prices; aggressive negotiations and value-based agreements can enhance reimbursement rates and sustain profitability.
4. How does market competition influence future price projections?
Increased competition from generics, biosimilars, or new therapies pressures existing prices downward, necessitating strategic adaptations for brand positioning.
5. When should companies consider pricing adjustments?
Pricing adjustments should be considered pre- and post-launch, especially in response to competitor entries, market uptake rates, and payer feedback.
References
- [Market Research Firm]. (2022). Global Therapeutic Market Analysis.
- [Industry Publication]. (2023). Pharmaceutical Pricing Trends.
- [FDA Records]. (2022). Drug Approvals and Patent Data.
- [Consulting Report]. (2023). Biosimilar Competition and Market Dynamics.
- [CMS Policy Paper]. (2023). Reimbursement and Value-Based Pricing.
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