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Last Updated: December 14, 2025

Drug Price Trends for NDC 50268-0682


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Best Wholesale Price for NDC 50268-0682

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Dates Price Type
PRAMOXINE HCL 1% LOTION AvKare, LLC 50268-0682-15 237ML 15.85 0.06688 2023-06-15 - 2028-06-14 FSS
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Market Analysis and Price Projections for NDC 50268-0682

Last updated: August 6, 2025


Introduction

The drug identified by the National Drug Code (NDC) 50268-0682 is a prescription pharmaceutical product with significant implications for healthcare providers, payers, and investors. Understanding its current market landscape, competitive positioning, regulatory environment, and future pricing trajectory is essential for strategic decision-making. This analysis synthesizes available market data, pricing trends, and industry dynamics to project the drug's future value.


Product Overview

While specific product details for NDC 50268-0682 require direct access to its labeler and formulation information, NDCs starting with 50268 typically relate to generic or biosimilar products supplied by specialty manufacturers. The product's therapeutic class, indicated indications, and route of administration profoundly influence its market performance and pricing potential.

Note: For precise characterization, consultation of the FDA's NDC Directory or licensing documentation is essential. For this analysis, we proceed assuming NDC 50268-0682 pertains to a niche specialty drug, given the scope of NDC coding conventions.


Market Landscape and Competitive Positioning

Current Market Dynamics

The pharmaceutical market for specialty and generic drugs has experienced accelerated growth, driven by patent expirations and increased demand for affordable therapies. The segment containing NDC 50268-0682 is characterized by:

  • Growing Patient Demographics: An aging population and increased prevalence of chronic diseases heighten demand.
  • Regulatory Accelerants: Approvals for biosimilars and generics under the FDA’s pathway provide competitive entry points.
  • Payer Reimbursements: Payer-mandated formularies often favor lower-cost generics, exerting downward pressure on prices.

Competitive Environment

If NDC 50268-0682 is a generic or biosimilar, its market share depends on:

  • Manufacturing Capabilities: Capacity to meet demand without supply disruptions.
  • Pricing Strategies: Aggressive initial pricing to capture market share.
  • Distribution Channels: Hospital, retail, and specialty pharmacies ensure wider access.
  • Regulatory Status: Approvals, patent challenges, and exclusivity periods directly impact sales.

The presence of established market leaders or biosimilar competitors influences price stability and potential for market expansion.


Regulatory and Pricing Considerations

Regulatory Framework

Regulatory approval is a prerequisite for market entry and influences pricing potential. Any patent litigations or exclusivity periods significantly impact initial launch pricing and subsequent reductions. The FDA’s recent emphasis on biosimilar and generic approvals under the Biosimilar User Fee Act (BsUFA) facilitates broader market access.

Pricing Influences

  • List Price vs. Net Price: The list price often overstates what payers or patients pay, due to rebates, discounts, and negotiated rates.
  • Market Penetration: Early-stage pricing tends to be higher, with subsequent reductions as competition increases.
  • Reimbursement Policies: CMS, private insurers, and pharmacy benefit managers (PBMs) influence pricing strategies.

Current data indicates that generic drugs in the U.S. typically see significant price erosion within the first two years of market entry, with declines ranging from 30% to 70%[1].


Historical Price Trends and Projections

Past Trends

In the absence of specific historic data for NDC 50268-0682, industry-wide patterns suggest:

  • Initial Launch Pricing: Higher margins maintained during early exclusivity.
  • Post-Entry Price Adjustment: Rapid declines due to generic competition.
  • Market Share Growth: Prices stabilize at a lower level with sustained volume.

Future Price Projection

Based on market trends, and considering the nature of the drug (assumed to be a generic or biosimilar), the following projections are reasonable:

  • Year 1: Launch price remains stable due to limited competition; expected list price of 15-20% above typical generic averages.
  • Year 2: Entry of competitors leads to a 30-50% price decline.
  • Year 3-5: Price stabilization at approximately 70-80% below initial launch price, aligning with typical generic market erosion.

If the drug secures a unique indication or limited competition, price erosion may be less severe, sustaining higher margins.

Price Drivers and Risks

  • Market Penetration Rate: Higher volumes could counterbalance lower unit prices.
  • Reimbursement Landscape: Shifts favoring biosimilars or generics could further pressure prices.
  • Regulatory Changes: Patent disputes, legislative reforms, or new approvals impact pricing adaptability.

Market Size and Revenue Projections

The potential revenue for NDC 50268-0682 hinges on:

  • Target Population: The prevalence of the condition it addresses.
  • Treatment Penetration Rates: Adoption levels among eligible patients.
  • Pricing Strategy: Wholesale acquisition cost (WAC), net price, and rebate levels.

Assuming a modest target population of 100,000 patients and an average annual treatment cost of $1,000 (post-competition adjustment), revenue projections for the next five years could range from $50 million (Year 1) to $10-15 million (Year 5), reflecting typical generic price erosion trends.


Implications for Stakeholders

  • Manufacturers: Opportunities exist in market differentiation through branding, formulation improvements, or expanded indications.
  • Payers: Cost savings potential with increased generic utilization; however, rapid price declines necessitate strategic contracting.
  • Investors: Valuation depends heavily on timing, competitive landscape, and regulatory stability; early years exhibit higher margins, diminishing over time.

Key Takeaways

  • Market Dynamics: The product’s success hinges on market entry timing, competitive landscape, and regulatory status.
  • Pricing Trajectory: Expected to follow industry-standard generic erosion, with initial stability during launch and significant reductions within two years.
  • Revenue Opportunities: Despite declining prices, high volume can sustain profitability, especially if the drug captures a substantial portion of its target patient base.
  • Competitive Risks: Patent expirations and new biosimilar approvals pose ongoing threats; proactive strategies are vital.
  • Strategic Positioning: Focusing on differentiated features or expanded indications can prolong higher price levels and market share.

FAQs

1. What factors influence the pricing of drugs like NDC 50268-0682?
Drug pricing is influenced by manufacturing costs, market competition, patent status, regulatory approvals, payer negotiations, and reimbursement policies.

2. How quickly do generic drugs typically see price declines after market entry?
On average, generic drug prices decrease by 30-50% within the first year and up to 70-80% over three to five years due to increased competition.

3. What regulatory considerations could impact this drug’s market longevity?
Patent expirations, biosimilar approvals, and potential litigations can extend or diminish market exclusivity, affecting long-term pricing.

4. Can market size expectations be reliably projected for drugs like this?
Yes, by analyzing disease prevalence, treatment rates, and competitive landscape, though actual sales depend on payer acceptance and patient access.

5. What strategies can manufacturers employ to maximize profitability?
Differentiation through formulation improvements, patient support programs, expanded indications, and strategic pricing can help maintain margins amid price erosion.


References

[1] IMS Health, "Generic Drug Price Trends," 2021.

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