You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: April 28, 2025

Drug Price Trends for NDC 81284-0152


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 81284-0152

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 NameVendorNDCCountPrice ($)Price/Unit ($)DatesPrice Type
PIPERACILLIN NA 3GM/TAZOBACTAM NA 0.375GM/VIL AvKare, LLC 81284-0152-10 10 50.01 5.00100 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
Showing 1 to 1 of 1 entries

Market Analysis and Price Projections for the Drug NDC: 81284-0152

Introduction

The National Drug Code (NDC) 81284-0152 identifies a specific drug product, and understanding its market dynamics and price projections involves several key factors. This analysis will delve into the current state of the pharmaceutical industry, pricing trends, and specific considerations for the drug in question.

Understanding the NDC

The NDC 81284-0152 is a unique 10-digit code that identifies the labeler, product, and trade package size of the drug. Here’s a breakdown of what each segment means:

  • Labeler Code: The first segment (81284) identifies the firm that manufactures, repacks, or distributes the drug.
  • Product Code: The second segment identifies the specific strength, dosage form, and formulation of the drug.
  • Package Code: The third segment identifies the package size and type[4].

Current Market Trends in the Pharmaceutical Industry

The pharmaceutical industry is facing several significant trends that can impact the pricing and market dynamics of any drug, including the one identified by NDC 81284-0152.

Pricing and Access

Pricing and access to drugs are among the most critical issues facing the life sciences industry. C-suite executives have identified these as significant challenges, with nearly half expecting these factors to significantly impact their strategies in 2025[2].

International Price Comparisons

Prescription drug prices in the U.S. are notably higher than in other high-income countries. For example, U.S. prices for brand-name drugs are 422% of prices in comparison countries, highlighting a substantial price disparity[3].

Generic and Biosimilar Competition

The rise of generic drugs and biosimilars is another key trend. Competition from these alternatives is expected to increase, with 37% of respondents viewing this as a top trend. This competition can drive down prices for branded drugs as patents expire[2].

Patent Cliff

The biopharma industry is facing a substantial loss of exclusivity due to expiring patents, with over $300 billion in sales at risk through 2030. This could lead to increased mergers and acquisitions as companies seek to maintain market share[2].

Specific Market Analysis for NDC 81284-0152

Drug Information Validation

To analyze the market for the drug identified by NDC 81284-0152, it is crucial to validate its information using the Drug Name and NDC Reference Data provided by the Centers for Medicare and Medicaid Services (CMS). This ensures that the drug information matches the CMS-approved dataset, which is essential for reporting payments and other regulatory compliance[1].

Pricing Considerations

Given the high prices of brand-name drugs in the U.S. compared to other countries, it is likely that the drug identified by NDC 81284-0152, if it is a brand-name drug, will be priced significantly higher than its counterparts in other high-income countries. However, if it is a generic or biosimilar, its pricing will be more competitive and potentially lower.

Market Competition

The presence of generic or biosimilar versions of the drug can significantly impact its market price. If the drug is facing competition from these alternatives, its price is likely to be lower. Conversely, if it enjoys market exclusivity, its price could remain higher.

Price Projections

Short-Term Projections

In the short term, the price of the drug identified by NDC 81284-0152 is likely to be influenced by current market trends and regulatory environments. If the drug is a brand-name product, it may maintain its high price due to the lack of immediate generic or biosimilar competition. However, if it is nearing the end of its patent life or already has generic competitors, prices may begin to decline.

Long-Term Projections

In the long term, several factors will influence the price:

  • Patent Expiration: If the drug's patent is set to expire, the introduction of generic or biosimilar versions will likely drive down prices.
  • Regulatory Changes: Changes in regulatory policies, such as those related to international price comparisons or reimbursement schemes, could impact pricing.
  • Market Competition: Increased competition from new entrants, including biosimilars and generic drugs, will continue to pressure prices downward.

Impact of Technological and Scientific Innovations

Drug Delivery Devices

Advances in drug delivery devices, particularly for biologics and peptides, could influence the market dynamics of the drug. If the drug in question benefits from new delivery methods, such as alternative routes of administration, it could enhance patient compliance and potentially affect pricing strategies[5].

Personalized Medicine

The trend towards personalized medicine, driven by advances in genomics and biomarkers, could lead to more precise treatment options. This might result in higher initial costs but could also reduce side effects and improve patient outcomes, potentially justifying higher prices in the long term[2].

Key Takeaways

  • Pricing Trends: U.S. prices for brand-name drugs are significantly higher than in other countries, but competition from generics and biosimilars can drive prices down.
  • Regulatory Compliance: Ensuring that drug information matches CMS-approved datasets is crucial for regulatory compliance.
  • Market Competition: The presence of generic or biosimilar versions can significantly impact the market price of the drug.
  • Technological Innovations: Advances in drug delivery devices and personalized medicine can influence market dynamics and pricing strategies.

FAQs

Q: What is the significance of the NDC in the pharmaceutical industry? A: The NDC is a unique code that identifies the labeler, product, and package size of a drug, ensuring accurate tracking and reporting.

Q: Why are U.S. drug prices higher than in other countries? A: U.S. drug prices are higher due to various factors, including lack of price controls, different reimbursement systems, and the influence of pharmaceutical companies on pricing.

Q: How does the patent cliff affect drug prices? A: The patent cliff leads to the loss of exclusivity for branded drugs, allowing generic and biosimilar versions to enter the market, which typically drives down prices.

Q: What role do drug delivery devices play in the pharmaceutical industry? A: Drug delivery devices can enhance patient compliance and outcomes, and innovations in this area can influence market dynamics and pricing strategies.

Q: How does personalized medicine impact drug pricing? A: Personalized medicine can lead to more precise and effective treatments, potentially justifying higher initial costs but also reducing side effects and improving patient outcomes in the long term.

Sources

  1. CMS: Drug Name and National Drug Code (NDC) Reference Data Instructions Calendar Year 2024.
  2. Deloitte Insights: 2025 life sciences outlook.
  3. ASPE: International Prescription Drug Price Comparisons: Estimates Using 2022 Data.
  4. FDA: National Drug Code Database Background Information.
  5. Drug Delivery Leader: 5 Reasons Why 2025 Is The Year Pharma Companies Will Revisit Their Drug Delivery Device Strategies.

More… ↓

⤷  Try for Free

Make Better Decisions: Try a trial or see plans & pricing

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. 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.