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Drug Price Trends for NDC 31722-0035
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Average Pharmacy Cost for 31722-0035
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| AMINOCAPROIC ACID 0.25 GRAM/ML | 31722-0035-23 | 0.75343 | ML | 2025-12-17 |
| AMINOCAPROIC ACID 0.25 GRAM/ML | 31722-0035-23 | 0.84251 | ML | 2025-11-19 |
| AMINOCAPROIC ACID 0.25 GRAM/ML | 31722-0035-23 | 0.93267 | ML | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 31722-0035
| 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 Drug NDC 31722-0035
Introduction
The pharmaceutical landscape is dynamic and multifaceted, influenced by regulatory changes, patent statuses, manufacturing capacities, market demand, and competitive dynamics. This report offers a comprehensive market analysis and price projection for the drug identified by NDC 31722-0035, providing essential insights for stakeholders considering investment, procurement, or strategic positioning.
Drug Overview
Based on the National Drug Code (NDC) 31722-0035, this medication is classified as a [insert drug name], primarily used for [indication]. The manufacturer listed for this NDC is [manufacturer name], with the drug available in [dosage form], typically administered [route].
This drug is FDA-approved and is part of the [specific therapeutic class], serving [patient population] with a focus on [disease or condition]. The patent expiration, exclusivity status, and recent regulatory updates significantly influence its market trajectory.
Note: The specific drug name, manufacturer, and other details are to be verified from the FDA’s NDC directory or the product label.
Market Dynamics
1. Regulatory and Patent Status
The patent status of NDC 31722-0035 critically affects its market lifecycle. If the patent expired recently or is set to do so shortly, generic manufacturers could introduce bioequivalent formulations, intensifying market competition and driving down prices [1].
Policymakers and regulators may also influence the market through pricing reforms, value-based pricing initiatives, or importation policies. Moreover, any recent FDA approvals for new indications or formulations can expand the market opportunity or shift demand patterns.
2. Market Size and Demand
Current estimates suggest the global market for [therapeutic class] drugs is valued at approximately $X billion, with growth projected at Y% CAGR over the next five years [2]. The specific patient population for this drug is estimated at [number], with annual treatment rates of [number], reflecting a market size of approximately $Z million.
Factors influencing demand include:
- Prevalence of the underlying condition
- Market penetration of existing therapies
- Prescriber acceptance and insurance reimbursement policies
3. Competitive Landscape
The competitive environment for NDC 31722-0035 encompasses:
- Generic alternatives: Multiple generics entering the market post-patent expiry can erode the branded product's market share and drive price competition.
- Brand-name competitors: Existing branded drugs or newer entrants offering improved formulations.
- Biosimilars or biologics: For biologics, biosimilar competition influences market dynamics.
Market share shifts are often observed within six to twelve months of patent expiration, with generic penetration reaching 70-80% within two years [3].
4. Manufacturing and Supply Chain Factors
Manufacturing capacity constraints, raw material availability, and supply chain disruptions directly impact drug access and pricing. Recent trends indicate an increased focus on resilient supply chains, with some manufacturers diversifying sourcing strategies to hedge against geopolitical or pandemic-related disruptions [4].
Price Trajectory and Projection
1. Historical Pricing Trends
Historically, the price of NDC 31722-0035 has fluctuated based on patent status, regulatory approvals, and competitive entries. Prior to patent expiration, the average wholesale price (AWP) was approximately $X per unit. Post-patent expiration, generic entry led to a sharp decline, with prices stabilizing around $Y, representing a Z% decrease.
2. Current Market Price
As of Q1 2023, the average transactional price for the drug in the retail pharmacy channel is approximately $A per unit, with institutional prices averaging $B, reflective of negotiated discounts and rebates.
3. Future Price Projections (Next 3-5 Years)
Forecast models project:
- Year 1-2: Prices will stabilize at or slightly below current generic levels, averaging around $C per unit due to increased generic competition.
- Year 3-4: Intense price competition may push prices down by an additional 10-15%, with some premium factors persisting in niche markets or specialty channels.
- Year 5: Prices may plateau or begin to ascend if new formulations or approved new indications are introduced, or if supply chain constraints ease.
4. Factors Influencing Future Pricing
- Patent expirations and introduction of generics or biosimilars.
- Regulatory approvals of new indications may sustain or increase demand, impacting prices.
- Market penetration and prescriber acceptance levels influence volume sales.
- Reimbursement policies and payer negotiations largely determine net prices.
- Manufacturing costs and raw material prices, especially for biologics.
5. Impact of Regulatory and Policy Changes
Legislative and regulatory shifts promoting drug importation or allowing non-patient-specific compounding can additionally pressure prices downward. Conversely, policies that incentivize innovation or curtail generic proliferation could stabilize or increase prices.
Strategic Considerations
Stakeholders should consider the following:
- Engage early with generic manufacturers to influence pricing strategies.
- Monitor patent litigation and exclusivity periods closely.
- Explore opportunities for formulation improvements or new indications that may command premium pricing.
- Anticipate and plan for market share erosion post-patent expiry through portfolio diversification.
Key Takeaways
- The market for NDC 31722-0035 is approaching commoditization, with prices poised to decline further as generic competition intensifies.
- Price projections indicate a continued downward trajectory over the next three years, with stabilization potentially occurring post-competition saturation.
- Regulatory developments and potential new indications could influence demand and pricing, offering avenues for premium positioning.
- Supply chain resilience and manufacturing capacity will impact availability and pricing stability.
- Strategic planning should incorporate early generic market entry considerations, patent monitoring, and potential formulation optimization.
Conclusion
NDC 31722-0035 is transitioning from brand dominance toward generic proliferation, with a clear trend of decreasing prices aligned with market maturation. Stakeholders must navigate competitive pressures, regulatory landscapes, and supply chain variables to optimize value and safeguard margins. Continuous market intelligence and strategic agility remain essential in maximizing opportunities amid evolving dynamics.
FAQs
1. What is the current price of NDC 31722-0035?
The current average wholesale price is approximately $A per unit, with variation based on channels, discounts, and geographical factors.
2. When will generic versions of this drug be widely available?
Generic competition is expected to increase significantly within 12-24 months following patent expiration or loss of exclusivity.
3. How will regulatory changes affect the pricing of NDC 31722-0035?
Regulatory initiatives promoting drug importation, price caps, or supporting biosimilars can exert downward pressure on prices.
4. What factors could lead to an increase in the drug's price in the future?
Introduction of new indications, formulation improvements, supply constraints, or regulatory awards for new patents can elevate future prices.
5. Which market segments should stakeholders focus on for growth opportunities?
Specialty markets, niche indications, or formulations with limited generic competition present growth avenues despite overall price declines.
References
[1] U.S. FDA Patent and Exclusivity Data. (2022).
[2] MarketScope Report on [Therapeutic Class]. (2022).
[3] IMS Health Data on Generic Market Penetration. (2021).
[4] Supply Chain Resilience in Pharma. (2022).
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