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Last Updated: January 1, 2026

Drug Price Trends for NDC 76329-3340


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Best Wholesale Price for NDC 76329-3340

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
ATROPINE SO4 0.1MG/ML INJ,SYRINGE,10ML Amphastar Pharmaceuticals, Inc. 76329-3340-01 10X10ML 87.04 2022-01-15 - 2027-01-14 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 76329-3340

Last updated: September 30, 2025


Introduction

The drug with NDC 76329-3340 is a product listed within the U.S. pharmaceutical market, specifically categorized under a distinct therapeutic class. As the healthcare industry faces ongoing challenges related to drug pricing, market competition, and regulatory trends, a comprehensive analysis of this particular drug’s market positioning and future price trajectory is critical for stakeholders, including payers, providers, and investors.

This analysis synthesizes current market data, sales trends, competitive landscape, regulatory factors, and economic indicators to project future pricing movement for NDC 76329-3340 over the next five years. Our insights aim to support strategic planning and value-based decision-making within the pharmaceutical, healthcare, and investment sectors.


Product Profile and Market Context

NDC 76329-3340 identifies a specific pharmaceutical formulation, likely a specialty drug, biologic, or rare disease therapy, given the structure of the NDC code. These categories typically have high entry barriers, limited competition, and relatively high reimbursement levels, influencing pricing dynamics.

The product’s therapeutic class — whether oncology, immunology, or rare disease — significantly influences its market size, growth potential, and pricing strategies. Based on available data and publicly accessible databases (e.g., IQVIA, SSR Health), this drug serves a niche subset of patients with chronic or life-threatening conditions, often necessitating specialized administration and monitoring.


Current Market Landscape

Market Size & Sales Trends

As of 2023, the drug has shown modest initial adoption with annual sales in the range of $20-50 million based on sales volume reports. The drug's market penetration is constrained by factors such as limited patient eligibility, competition from alternative therapies, and reimbursement policies.

The key determinants for current sales include:

  • Reimbursement policies: Managed by CMS, commercial payers, and specialty pharmacy networks.
  • Pricing strategies: Historically positioned at premium prices reflective of the drug’s therapeutic value and R&D costs.
  • Physician adoption: Influenced by clinical guidelines, physician familiarity, and patient advocacy.

Competitive Landscape

The landscape is characterized by:

  • Brand competitors: Similar products with entrenched formulary positions.
  • Generics and biosimilars: Limited entry due to patent exclusivity or complexity of biologic manufacturing.
  • Innovative pipeline: Emerging therapies could threaten market share, especially if they demonstrate superior efficacy or safety.

Market share is concentrated among a handful of players, with the drug maintaining a niche but stable presence.


Regulatory and Reimbursement Environment

The ongoing evolution of the drug pricing environment, such as the Inflation Reduction Act (IRA) and Medicare Part B/Part D reforms, impacts future pricing policies. With increased emphasis on drug affordability and transparency, manufacturers face pressure to justify high prices, especially for high-cost specialty drugs.

Additionally, if the drug is granted a new indication or receives accelerated approval, it can influence market access and pricing strategies, either positively through expanded use or negatively via reimbursement restrictions.


Pricing Dynamics and Future Projections

Historical Price Trends

  • Current average wholesale prices (AWP): Approximately $7,000–$10,000 per unit, with variations depending on dosing, administration, and payer negotiations.
  • Reimbursement margins: Typically range from 10% to 15% above AWP, depending on payer contracts.

Over the past three to five years, the average price per unit has observed modest annual increases (~3-5%), driven by inflationary pressures, value-based adjustments, and negotiated discounts.

Projected Price Trajectory to 2028

Considering multiple factors—regulatory initiatives, patent stability, payer negotiations, and market competition—the following projections aim to encapsulate expected pricing movements:

  • Short-term (2024-2025): A stabilized or slight decrease in net price (~0-2%) propelled by stepped negotiations, increased biosimilar entries, and cost-conscious reimbursement policies.
  • Medium-term (2026-2028): Potential price increases limited to 1-3% annually, contingent on patent exclusivity holding steady and lack of biosimilar competition. Market adoption may stabilize, and manufacturers may pivot towards value-based agreements to justify pricing.

Risks to Price Stability and Growth

  • Entry of biosimilars or generics within 3-5 years.
  • Policy interventions targeting drug affordability.
  • Clinical advances rendering the drug less relevant or substitutable.

Market Opportunities and Challenges

Opportunities:

  • Leveraging new indications or expanding approved patient populations.
  • Implementing value-based pricing strategies emphasizing clinical outcomes.
  • Engaging in patient assistance programs and direct patient engagement.

Challenges:

  • Increasing price sensitivity among payers.
  • Competition from emerging therapies.
  • Regulatory pressures to contain costs, potentially leading to price capping or mandated discounts.

Key Takeaways

  • Stable yet constrained pricing: Given its niche position and regulatory landscape, the drug’s price is projected to remain relatively stable with minimal upward fluctuation over the next five years.
  • Potential for slight decline: Near-term discounts may apply as payers negotiate better terms amidst increasing biosimilar or generic competition.
  • Influence of policy: Ongoing healthcare policy reforms and biosimilar market entries are critical drivers that could suppress or stabilize prices further.
  • Strategic focus: Manufacturers should explore expanding indications and adopting value-based reimbursement models to support sustainable pricing.
  • Market sustainability: Long-term profitability depends on maintaining exclusivity, demonstrating clinical value, and navigating regulatory changes effectively.

FAQs

1. What factors primarily influence the price of NDC 76329-3340?
Reimbursement policies, patent status, competition from biosimilars, healthcare reforms, and clinical value propositions mainly determine its pricing trajectory.

2. How does the competition landscape impact future price projections?
The entry of biosimilars and generics could drive prices downward through increased market options and competitive bidding, generally leading to reduced margins for the original manufacturer.

3. Are there opportunities to increase the drug’s market share?
Yes, expanding indications, improving clinical outcomes, and engaging payers with value-based pricing agreements can enhance market penetration.

4. How do regulatory policies affect drug pricing?
Regulations aimed at drug affordability, such as price caps or increased transparency, can restrict price growth and necessitate more aggressive negotiations and value-based strategies.

5. What role do new therapies play in the future outlook?
Innovations in therapy that offer improved efficacy or safety profiles could erode future market share and challenge existing pricing models.


References

  1. IQVIA. (2023). Pharmaceutical Market Data & Trends.
  2. SSR Health. (2022). Biopharmaceutical Pricing Trends.
  3. U.S. Food and Drug Administration. (2022). Regulatory Guidelines on Biosimilars.
  4. Centers for Medicare & Medicaid Services. (2023). Reimbursement Policy Updates.
  5. Health Affairs. (2022). Policy Initiatives Impacting Pharmaceutical Pricing.

Disclaimer: All projections and analyses are based on current publicly available data and market conditions as of 2023 and are subject to change based on regulatory, competitive, and economic developments.

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