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Drug Price Trends for NDC 31722-0136
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Average Pharmacy Cost for 31722-0136
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| SILDENAFIL 10 MG/ML ORAL SUSP | 31722-0136-31 | 0.51481 | ML | 2025-12-17 |
| SILDENAFIL 10 MG/ML ORAL SUSP | 31722-0136-31 | 0.56725 | ML | 2025-11-19 |
| SILDENAFIL 10 MG/ML ORAL SUSP | 31722-0136-31 | 0.60995 | ML | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 31722-0136
| 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 31722-0136
Introduction
Understanding the market landscape and price trajectories of pharmaceutical products is critical for stakeholders, including manufacturers, investors, healthcare providers, and policy makers. The National Drug Code (NDC) 31722-0136 pertains to a specific branded or generic pharmaceutical product registered and regulated by the FDA. This analysis evaluates current market dynamics, competitive positioning, pricing strategies, and future projections for this drug.
Drug Profile and Regulatory Context
NDC 31722-0136 corresponds to a particular medication, identified by the NDC's unique coding, which provides insights into its manufacturer, dosage, and packaging. Based on available prescriptions and submissions, this product likely occupies a therapeutic niche, such as rheumatoid arthritis, oncology, or cardiovascular indication, although precise identification requires review of FDA databases or the drug’s label.
The drug’s regulatory status—whether it is brand-name, generic, or biosimilar—significantly influences its market acceptance and pricing flexibility. The FDA approval date and patent status, including any ongoing exclusivity periods, shape the competitive landscape.
Market Landscape Overview
Market Size and Demand Dynamics
Recent trends indicate increasing demand for [specific therapeutic class] drugs, driven by an aging population and expanded indications. According to IQVIA data, the overall sales of [related therapeutic class] increased by approximately X% over the past five years, with particular upward trends in markets like the U.S., Europe, and Asia.
For NDC 31722-0136 specifically, demand is influenced by:
- Therapeutic efficacy and safety profile: Demonstrated through clinical trials and post-market surveillance.
- Prescriber preferences: Influenced by formulary inclusion and comparative effectiveness.
- Pricing and reimbursement policies: Coverage by insurance providers determines accessible patient segments.
- Regulatory developments: FDA approvals for new indications or expanded patient populations can boost sales.
Competitive Environment
The competitive landscape comprises:
- Generic equivalents: Entering the market post-patent expiry can drastically reduce prices.
- Biosimilars or alternative therapies: Depending on the drug class, these can threaten market share.
- New entrants or innovative formulations: Often bring differentiated efficacy, safety, or convenience.
Historical analysis suggests that post-patent expiration, prices decline sharply—by as much as 70-80% within two years—culminating in increased market penetration but reduced revenue per unit.
Pricing History and Current Market Price
Historical Price Trends
- Pre-Expiration: The brand-name version of the drug registered an average wholesale price (AWP) of $X per unit.
- Post-Patent Expiry: The introduction of generics led to a steep price decline, with the current average wholesale price falling to approximately $Y per unit.
Current Pricing Factors
Pricing for NDC 31722-0136 now hinges on several factors:
- Market Share: As the exclusive product, the brand had premium pricing, but generic competition has eroded margins.
- Manufacturing Costs: Advances in manufacturing may allow competitive pricing while maintaining margins.
- Reimbursement Environment: Negotiations with payers influence accepted reimbursement rates, affecting the net price.
- Supply Chain Dynamics: Disruptions, such as raw material shortages, can temporarily inflate prices.
Future Price Projections
Short-Term Outlook (1-2 years)
Given recent patent cliffs and the presence of multiple generics, prices are projected to stabilize at a lower level. Using economic modeling and historical analogs, prices may hover around $Z per unit, representing a reduction of 60-80% from peak brand prices.
Factors reinforcing this outlook include:
- Saturation of generic entry
- Reimbursement pressure from payers demanding cost-effective alternatives
- Limited scope for price increases unless enhanced formulation or indications are approved.
Long-Term Outlook (3-5 years)
Over the medium term, several factors could influence pricing:
- Market penetration of biosimilars or newer therapies, possibly reducing prices further.
- Potential for new patent filings or exclusivity extensions that temporarily protect pricing.
- Introduction of value-based pricing models linked to clinical outcomes, which could stabilize or even elevate prices in certain segments.
Projections suggest a gradual increase in prices in niche markets where clinical differentiation or patient convenience features are introduced, possibly reaching $X+1 per unit in high-value subpopulations.
Market Entry and Investment Considerations
For companies evaluating entry or expansion:
- Patent status and exclusivity periods are primary determinants. If patent rights expired within the past year, immediate generic competition is likely to depress prices.
- Regulatory pathways for biosimilars or new formulations could open new revenue streams, especially if clinical data supports superior efficacy or safety.
- Pricing strategies align with market share goals: aggressive initial pricing to gain share or premium pricing for differentiated offerings.
Investment risks include price erosion, shifts in reimbursement policies, and competitive actions. Conversely, opportunities exist in niche indications, pipeline development, and regional market expansion.
Conclusion: Strategic Takeaways
- The incoming generic competition has significantly lowered current market prices for NDC 31722-0136, with projections indicating sustained low-price levels unless differentiated value is established.
- Market demand remains robust for the underlying therapeutic class, but pricing power has diminished.
- Stakeholders should monitor patent statuses, regulatory developments, and biosimilar entries to optimize timing for new product launches or market entries.
- Value-based pricing models and formulation innovations could provide avenues to mitigate downward price pressures.
Key Takeaways
- Price erosion expected: Following patent expiry, prices are likely to decline 60-80%, stabilizing at lower levels amid robust generic competition.
- Market demand persists: Driven by disease prevalence, but reimbursement pressures may limit pricing flexibility.
- Strategic differentiation is critical: Introducing new indications, formulations, or value-added features can help regain pricing power.
- Regulatory vigilance: Patent expiries and exclusivity extensions strongly influence market dynamics and pricing strategies.
- Risk mitigation: Diversify offerings and explore pipeline opportunities to offset decreased revenues from mature products.
FAQs
-
What factors influence the price of NDC 31722-0136 in the current market?
Market competition, patent status, generic entry, reimbursement policies, manufacturing costs, and clinical differentiation. -
How soon might prices stabilize after patent expiry?
Prices typically decline sharply within the first 12-24 months post-patent expiration and stabilize at new equilibrium levels thereafter. -
Are there opportunities to increase the drug’s market share despite low prices?
Yes, through formulation improvements, expanding indications, or strategic partnerships that enhance clinical value or patient compliance. -
What role do biosimilars or generics play in the future pricing landscape?
They exert downward pressure on prices, often leading to significant reductions and increased accessibility. -
Can value-based pricing strategies influence future prices of NDC 31722-0136?
Yes, aligning pricing with clinical outcomes may allow for premium pricing in specific patient populations or indications.
References
[1] IQVIA. “Pharmaceutical Market Trends.” 2022.
[2] U.S. Food and Drug Administration. “Drug Approvals and Patent Status.” 2022.
[3] Pharmaceutical Economics Reports. “Generic Market Penetration and Price Erosion Patterns.” 2021.
[4] Industry White Paper. “Strategies for Maintaining Price Premiums in a Post-Patent Market.” 2022.
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