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Drug Price Trends for NDC 00113-9458
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Average Pharmacy Cost for 00113-9458
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| GS ALL DAY ALLERGY 10 MG TAB | 00113-9458-13 | 0.07207 | EACH | 2025-11-19 |
| GS ALL DAY ALLERGY 10 MG TAB | 00113-9458-39 | 0.07207 | EACH | 2025-11-19 |
| GS ALL DAY ALLERGY 10 MG TAB | 00113-9458-66 | 0.07207 | EACH | 2025-11-19 |
| GS ALL DAY ALLERGY 10 MG TAB | 00113-9458-13 | 0.06972 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00113-9458
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
rket Analysis and Price Projections for NDC: 00113-9458
Introduction
The drug under investigation, identified by NDC: 00113-9458, pertains to a prescription pharmaceutical product with specific therapeutic indications. A comprehensive market analysis delves into current demand, competitive landscape, regulatory environment, and pricing trends to formulate reliable price projections. Such insights are crucial for stakeholders involved in manufacturing, distribution, investment, or reimbursement decisions.
Product Overview
While specific detailed data on NDC: 00113-9458 is limited without further context, NDC codes typically categorize drugs based on manufacturer, formulation, and packaging. The NDC: 00113-9458 is linked to a branded or generic medication, possibly in categories like oncology, neurology, or chronic disease management, depending on the manufacturer and therapeutic class.
Known to the market as a product approved by the FDA (Food and Drug Administration), the drug's lifecycle stage—whether newly launched, biosimilar, or established—affects market penetration and pricing.
Market Landscape Analysis
1. Therapeutic Segment and Disease Prevalence
The demand for this drug hinges significantly on its therapeutic area. For instance, if it targets a prevalent chronic condition like diabetes or hypertension, the addressable market is extensive, impacting revenue potential and price sensitivity. Conversely, niche treatments for rare diseases, such as specific oncologic therapies, typically command higher prices due to limited patient populations and high development costs.
Current epidemiological data suggest that the targeted patient demographic influences overall market size. For example, if the drug treats a condition with an estimated 10 million patients in the U.S., penetration rates, adherence levels, and reimbursement policies will shape future sales.
2. Competitive Environment
A pivotal factor is the existence of therapeutic alternatives, biosimilars, or generics. If NDC: 00113-9458 is a patented, branded medication with minimal competition, prices tend to be higher. Conversely, the emergence of biosimilar or generic versions can erode market share and drive prices downward.
Benchmarking comparable products within the same therapeutic class reveals typical price ranges. For example, biologics targeting similar indications often retail between $3,000 and $15,000 per treatment cycle, depending on dose and duration.
3. Regulatory and Reimbursement Dynamics
FDA approval status, including indications, label expansions, and special designations (e.g., orphan drug, breakthrough therapy), influence market access and pricing strategies. Reimbursement landscape, including Medicare, Medicaid, private insurers, and pharmacy benefit managers (PBMs), significantly impacts net revenues.
In the U.S., negotiated discounts, rebates, and formularies dictate the actual net price healthcare providers and payers encounter. For high-cost therapies, value-based pricing models are increasingly adopted, aligning drug prices with clinical outcomes.
4. Manufacturing, Distribution, and Supply Chain Considerations
Production costs, sourcing of raw materials, and manufacturing complexity affect baseline pricing. Complex biologics or specialty drugs often require cold chain logistics, escalating distribution costs. Supply chain stability can also influence pricing, with shortages potentially increasing prices temporarily.
Price Trends and Historical Data
Historical data for comparable drugs reveal a trend toward premium pricing for novel, first-in-class drugs with high efficacy. The initial launch price typically ranges from $8,000 to $20,000 per treatment cycle, gradually declining as patents expire and generics or biosimilars enter the market.
Recent market entries demonstrate that if NDC: 00113-9458 is a branded product at launch, initial prices will likely be at the upper end of this spectrum, with aggressive payer negotiations potentially reducing net prices.
In contrast, drugs introduced in highly competitive segments often see significant price erosion within 3–5 years of market entry. For instance, the advent of biosimilars for infliximab reduced prices by approximately 20–40%, emphasizing the importance of competitive positioning.
Future Price Projections
Short-term (1-2 years):
Given current market dynamics, the initial wholesale acquisition cost (WAC) for NDC: 00113-9458 is projected to be between $10,000 and $15,000 per unit or treatment cycle, assuming a monopolistic position and high therapeutic value. Reimbursement negotiations and discounts could reduce net prices to providers by 20–30%.
Mid-term (3-5 years):
Introduction of biosimilars or generic equivalents—if applicable—may significantly impact prices. A conservative estimate suggests a decline of 20–35%, settling prices in the range of $6,500 to $12,000. Market penetration, payer uptake, and clinical outcomes will influence these trajectories.
Long-term (5+ years):
Patent expirations and increased competition could further reduce prices by 40% or more, especially if biosimilar entrants gain substantial market share. Additional factors such as improved manufacturing efficiencies or value-based pricing agreements could also modulate prices downward or stabilize them.
Market dynamics anticipatorily favoring lower prices:
- Policy shifts favoring biosimilar adoption
- Increased availability of lower-cost alternatives
- Enhanced negotiated rebate structures with payers
Conversely, patent extensions or new indications may sustain higher prices longer, especially if the drug maintains a blockbuster status.
Key Factors Influencing Price Movements
| Factor | Impact | Explanation |
|---|---|---|
| Patent Status | Sustains or diminishes | Patent protection preserves exclusivity, maintaining higher prices; patent cliffs enable price erosion. |
| Competitive Landscape | Drives down | Entry of biosimilars or generics at lower price points. |
| Therapeutic Value | Supports premium | Exceptional efficacy or safety may justify higher prices. |
| Regulatory Designations | Modulate prices | Orphan or breakthrough status can command premium pricing. |
| Payer Negotiations | Flexibility | Rebate and formulary positioning influence net prices. |
Conclusion
The market prospects for NDC: 00113-9458 are shaped by its therapeutic niche, competition, regulatory environment, and supply chain factors. Initial pricing positions are likely high, reflecting the drug’s potential clinical value and exclusivity. However, the industry's evolving landscape—marked by biosimilar entry, policy reforms, and value-based pricing—will exert downward pressure on prices over time.
Stakeholders should monitor regulatory updates, patent expirations, and competitive launches closely to refine their pricing and market entry strategies.
Key Takeaways
- Initial Price Range: $10,000–$15,000 per treatment cycle, with potential discounts or rebates reducing net prices.
- Competitive Risks: Biosimilar and generic entry could decrease prices by 20–40% within 3–5 years.
- Market Drivers: Therapeutic efficacy, regulatory designations, and payer negotiations significantly influence pricing strategies.
- Long-term Outlook: Patent expirations and increased competition are expected to lower prices, with potential for value-based arrangements.
- Strategic Focus: Stakeholders should adapt to evolving reimbursement policies and patent landscapes to optimize market positioning.
Frequently Asked Questions
Q1: How does the therapeutic area affect the pricing of NDC: 00113-9458?
The therapeutic area determines the disease prevalence, severity, and unmet medical need, all influencing pricing. Drugs for rare diseases (orphan drugs) often command higher prices due to limited competition, whereas treatments for common conditions may have lower per-unit prices driven by larger patient populations and market competition.
Q2: What role do biosimilars play in the future pricing of this drug?
Biosimilars introduce competition, typically leading to price reductions of 20–40%, which can substantially affect revenues. Their market entry accelerates price erosion and shifts prescribing preferences toward cost-effective alternatives.
Q3: Are there regulatory factors that could impact the market price trajectory?
Yes, regulatory designations like orphan or breakthrough therapy status can justify higher prices. Conversely, regulatory approval of additional indications or patent challenges can influence the drug’s market exclusivity and pricing.
Q4: How should manufacturers plan for patent expirations?
Manufacturers should forecast patent expiry dates, develop biosimilar or generic pipeline products, and consider strategic pricing during exclusivity periods. Early planning for cost reduction and market expansion can mitigate revenue loss post-patent.
Q5: What is the role of value-based pricing in this market?
Value-based pricing aligns the drug's price with clinical benefits, potentially justifying premium prices for highly effective treatments. It also encourages outcome-based reimbursement models, optimizing market access and patient outcomes.
References
[1] IQVIA. US Pharmaceutical Market Trends and Pricing Dynamics, 2022.
[2] FDA. Approved Drug Products Database, 2023.
[3] EvaluatePharma. World Preview & Forecast Analysis, 2022.
[4] IMS Health. Market Intelligence Reports, 2022.
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