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Last Updated: April 6, 2025

Drug Price Trends for NDC 72603-0212


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Average Pharmacy Cost for 72603-0212

Drug NameNDCPrice/Unit ($)UnitDate
DEXAMETHASONE 0.5 MG TABLET 72603-0212-01 0.09635 EACH 2025-03-19
DEXAMETHASONE 0.5 MG TABLET 72603-0212-01 0.09796 EACH 2025-02-19
DEXAMETHASONE 0.5 MG TABLET 72603-0212-01 0.09767 EACH 2025-01-22
DEXAMETHASONE 0.5 MG TABLET 72603-0212-01 0.09289 EACH 2024-12-18
DEXAMETHASONE 0.5 MG TABLET 72603-0212-01 0.09507 EACH 2024-11-20
DEXAMETHASONE 0.5 MG TABLET 72603-0212-01 0.08516 EACH 2024-10-23
DEXAMETHASONE 0.5 MG TABLET 72603-0212-01 0.07559 EACH 2024-09-18
>Drug Name>NDC>Price/Unit ($)>Unit>Date
Showing 1 to 7 of 7 entries

Best Wholesale Price for NDC 72603-0212

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
No data available in table
>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 0 to 0 of 0 entries

Market Analysis and Price Projections for the Drug NDC: 72603-0212

Introduction

The pharmaceutical market is a complex and dynamic sector, influenced by various factors including technological advancements, regulatory changes, and market demand. This article focuses on the market analysis and price projections for a specific drug identified by the NDC code 72603-0212, although the provided sources do not directly mention this NDC code. We will, however, use relevant industry trends and data from similar drugs to infer potential market dynamics.

Understanding NDC Codes

National Drug Codes (NDCs) are unique identifiers assigned to pharmaceutical products. Each NDC code provides detailed information about the drug, including its manufacturer, dosage form, and packaging[2].

Market Context: Biopharma and Biotech Industries

The biopharma and biotech industries are experiencing rapid growth, driven by advancements in technology, evolving regulatory frameworks, and a shift towards patient-centered care. By 2025, the biopharma market is projected to grow at a compound annual growth rate (CAGR) of 7.56%, while the biotech sector is expected to grow at a CAGR of 9.4% between 2021 and 2027[3].

Drug Development and Clinical Trials

Accelerated clinical trial designs are becoming more prevalent, aiming to reduce the time and cost associated with drug development. This trend is expected to continue in 2025, with a focus on innovative study designs and more efficient timelines[3].

Specific Market Analysis: Oncology and Targeted Therapies

Given the lack of direct information on the NDC code 72603-0212, we can look at the broader market trends in oncology and targeted therapies for insights. The non-small cell lung cancer (NSCLC) market, for example, is expected to grow significantly due to the increasing use of immune checkpoint inhibitors and targeted therapies.

Immune Checkpoint Inhibitors

Drugs like Keytruda (pembrolizumab), Opdivo (nivolumab), and Tecentriq (atezolizumab) are projected to dominate the NSCLC market, with combined sales of $17.5 billion by 2025. These immunotherapies are driving growth in the oncology sector[4].

Targeted Therapies

Targeted therapies, such as AstraZeneca’s Tagrisso (osimertinib) and Roche’s Avastin (bevacizumab), are also expected to contribute significantly to the NSCLC market. Tagrisso, for instance, is projected to achieve blockbuster status with estimated sales of $1.7 billion by 2025, driven by its uptake in EGFR-mutant patients[4].

Price Projections and Market Dynamics

While specific price projections for the NDC code 72603-0212 are not available, we can infer from the broader market trends:

Impact of Patent Expirations

The expiration of patents for blockbuster drugs can significantly impact market dynamics. For example, the patent expiration of Tarceva and Alimta has led to a decline in their sales, with generic alternatives filling the gap. This trend suggests that drugs with expiring patents may see a drop in prices and market share[4].

Premium-Priced Therapies

Premium-priced therapies, especially in the oncology sector, continue to drive market growth. However, their high costs can limit uptake, especially in combination therapies. For instance, the combination of durvalumab and tremelimumab is expected to lag behind monotherapy and IO + chemotherapy combinations due to its high cost[4].

Regulatory Landscape

The regulatory landscape is evolving to keep pace with innovation. This includes more flexible and adaptive clinical trial designs, which can influence the pricing and market positioning of new drugs. Regulatory approvals and label expansions can significantly impact the market share and pricing of drugs[3].

Patient-Centered Care

There is a growing focus on patient-centered care, which includes personalized medicine and more efficient clinical trials. This shift can lead to better patient outcomes and potentially more competitive pricing as drugs are tailored to specific patient needs[3].

Key Takeaways

  • Market Growth: The biopharma and biotech industries are experiencing rapid growth driven by technological advancements and evolving regulatory frameworks.
  • Oncology Market: Immune checkpoint inhibitors and targeted therapies are driving growth in the NSCLC market.
  • Price Dynamics: Patent expirations can lead to a decline in sales for blockbuster drugs, while premium-priced therapies continue to dominate the market.
  • Regulatory Changes: Adaptive clinical trial designs and evolving regulatory frameworks are shaping the future of drug development and pricing.
  • Patient-Centered Care: There is a growing focus on personalized medicine and patient-centered care, which can influence market dynamics.

FAQs

  1. What is the significance of NDC codes in the pharmaceutical industry? NDC codes are unique identifiers that provide detailed information about a drug, including its manufacturer, dosage form, and packaging. This helps in tracking and managing pharmaceutical products efficiently.

  2. How are accelerated clinical trial designs impacting drug development? Accelerated clinical trial designs are reducing the time and cost associated with drug development by promoting more efficient timelines and avoiding exposure to ineffective therapies.

  3. What are the key drivers of growth in the NSCLC market? The NSCLC market is driven by the increasing incorporation of premium-priced immune checkpoint inhibitor immunotherapies and targeted therapies.

  4. How do patent expirations affect the market share of drugs? Patent expirations can lead to a decline in sales for blockbuster drugs as generic alternatives enter the market, reducing the market share and prices of the original drugs.

  5. What role does patient-centered care play in the biopharma and biotech industries? Patient-centered care, including personalized medicine and more efficient clinical trials, is becoming a focal point, leading to better patient outcomes and potentially more competitive pricing.

Sources

  1. SEER Cancer Statistics Review: Doxorubicin Hydrochloride - CanMED: NDC[1]
  2. CDC: IIS | Code Sets | NDC | Vaccines[2]
  3. TFS CRO: 5 Predictions for the Biopharma and Biotech Industries in 2025[3]
  4. GlobalData: NSCLC MARKET - Global Drug Forecast & Market Analysis to 2025[4]
  5. DailyMed: METOPROLOL SUCCINATE tablet, extended release[5]

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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. 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.