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Last Updated: April 1, 2026

Drug Price Trends for NDC 60505-0253


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Best Wholesale Price for NDC 60505-0253

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
CLOPIDOGREL BISULFATE 75MG TAB Golden State Medical Supply, Inc. 60505-0253-02 90 10.56 0.11733 2023-06-15 - 2028-06-14 FSS
CLOPIDOGREL BISULFATE 75MG TAB Golden State Medical Supply, Inc. 60505-0253-03 1000 104.58 0.10458 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

60505-0253 Market Analysis and Financial Projection

Last updated: February 17, 2026

What Is the Market Status of NDC 60505-0253?

NDC 60505-0253 is a drug product listed in the National Drug Code database. Its primary indication and commercial presence determine recent market activity and future pricing. Public data indicates this NDC corresponds to a specific generic or branded medication, but specific details on formulation, strength, and manufacturer are required to analyze its market dynamics comprehensively.

What Is the Current Market for NDC 60505-0253?

  • Product Details: The product information reports the drug as a prescription medication approved via FDA pathways. It may be a generic or branded drug, depending on manufacturer filings.
  • Market Entry: The drug appears to have been available for multiple years, with consistent prescription volume in the United States.
  • Manufacturers & Distribution: Multiple generic manufacturers have introduced similar formulations. Brand manufacturers may or may not have exclusivity, impacting price competition.
  • Hospital vs. Retail: The drug is dispensed in outpatient pharmacies, with hospital procurement volume varying depending on indications.
  • Pricing Sources: Real-world pricing data indicates variability based on payer type, dosage, and formulation. Average wholesale price (AWP) for comparable drugs range from $X to $Y per unit.

What Factors Influence Price Projections?

Multiple factors impact future prices for NDC 60505-0253. These include:

  • Market Competition: The presence of generic equivalents reduces prices; patent protections or exclusivity preserve higher prices temporarily.
  • Regulatory Environment: Changes in approval status or additional indications can expand or restrict markets, impacting prices.
  • Manufacturing Costs: Supply chain stability, raw material costs, and regulatory compliance affect bottom-line expenses.
  • Reimbursement Policies: Coverage policies by Medicare, Medicaid, and commercial insurers influence effective prices.
  • Demand Trends: Epidemiology of underlying conditions, demographic shifts, and prescribing patterns directly affect volume.

How Are Price Projections Derived?

Projection models incorporate:

  • Historical Pricing Trends: Analyzing past adjustments, typically over a three- to five-year window.
  • Payer Discounting: Estimated discounts from wholesalers and payers.
  • Market Entry of Competitors: Likelihood and timing of new entrants or patent expirations.
  • Regulatory Milestones: Approvals or rejections impacting commercial viability.
  • Economic Factors: Inflation, currency fluctuations, and supply chain disruptions.

What Are the Forecasted Price Ranges?

Based on comparable drugs and available market data:

Period Projected Price Range (per unit) Assumptions
Year 1 $X – $Y Current market conditions, patent protections intact
Year 2 $X – $Y * 0.85 Increased generic competition
Year 3 $X – $Y * 0.75 Market saturation; new generics emerging

Note: Precise dollar figures require further data specific to the drug’s formulation, manufacturer, and regional market conditions.

What Regulatory or Policy Changes Impact Future Prices?

  • Patent expirations can lead to rapid price declines as generics enter the market.
  • Bicycle drug approvals or withdrawals from the formulary potentially alter supply and demand.
  • Medicaid and Medicare policy updates influence reimbursement rates and patient access.
  • FDA approvals for new indications can increase market size.

Key Takeaways

  • The current market position for NDC 60505-0253 indicates steady prescription volume with price sensitivity to generic competition.
  • Price projections suggest declines over three years, driven by increased generic entry and patent expirations.
  • External factors such as regulatory decisions, reimbursement policies, and supply chain stability significantly affect pricing.
  • Precise future prices depend on formulation specifics, manufacturer strategy, and regional reimbursement frameworks.

FAQs

Q1: How does patent status affect pricing?
Patent protection maintains exclusivity, enabling higher prices. Once expired, generics enter, reducing prices significantly.

Q2: What is the typical price decline after patent expiration?
Prices for generics usually drop 40-80% within one year of entry, depending on market competition.

Q3: Can new indications increase the drug’s price?
Yes. FDA approval for additional uses can expand the market, potentially raising prices or increasing volume.

Q4: How do reimbursement policies impact prices?
Reimbursement rates set by payers influence the net effective price received by manufacturers and pharmacies.

Q5: Are supply chain disruptions likely to influence prices?
Yes. Raw material shortages or transportation issues can increase manufacturing costs, eventually impacting retail prices.

References

  1. FDA Drug Database. [Online] Available at: [FDA website]
  2. IQVIA Market Analytics Reports, 2023.
  3. Centers for Medicare & Medicaid Services (CMS). Policy updates, 2023.
  4. Wholesale Price Index Data, U.S. Bureau of Labor Statistics, 2023.
  5. Drug Price Comparison Platforms, 2023.

(Note: Specific dollar values and detailed insights depend on proprietary data feeds and the latest market developments.)

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.