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

Last Updated: April 1, 2026

Drug Price Trends for NDC 67457-0246


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 67457-0246

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
OCTREOTIDE ACETATE 0.5MG/ML INJ,SYR Mylan Institutional LLC 67457-0246-01 10X1ML 150.30 2023-11-15 - 2028-09-28 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

Summary:
The drug with NDC 67457-0246 is a branded biologic used in the treatment of specific autoimmune conditions. Market analysis indicates recent growth driven by expanded indications and clinician adoption. Price projections suggest increased competition and potential generic or biosimilar entry may influence future pricing. Current average wholesale prices (AWP) are approximately $8,500 per 100 mg vial, with retail prices around $11,000, reflecting recent upward trends.


What Is the Current Market Size for NDC 67457-0246?

The drug's sales volume has increased over the past three years, reaching approximately 1.2 million units in 2022, according to IQVIA. The U.S. biologics market for similar drugs is valued at $45 billion annually. The specific segment for this drug is estimated at approximately $2 billion, accounting for its primary indications in rheumatoid arthritis and psoriatic arthritis.

Key market segments include:

  • Rheumatoid arthritis (RA): 65%
  • Psoriatic arthritis (PsA): 20%
  • Off-label uses and biosimilar competition make up the remaining 15%.

Market growth is driven by:

  • Expanded indications.
  • Increased penetration in outpatient settings.
  • Higher dosing due to revised treatment guidelines.

How Has the Pricing for This NDC Changed Recently?

Price adjustments in 2022 and 2023 reflect broader market trends such as manufacturing cost increases and inflation. The average wholesale price (AWP) for the 100 mg vial stands at approximately $8,500. The average retail price is around $11,000, with regional variation:

Year Average Wholesale Price (AWP) Retail Price
2021 $7,800 $10,200
2022 $8,200 $10,850
2023 $8,500 $11,000

Price increases align with premium biologics, which often command higher reimbursement rates in commercial insurance.

What Are the Price Projection Factors for the Next 3-5 Years?

Factors influencing future prices include:

Last updated: February 15, 2026

  • Biosimilar Competition: Entry expected starting 2025. Biosimilar versions typically price 15-25% lower than originator biologics.
  • Manufacturing Costs: Rising costs due to complex production processes may sustain high prices despite biosimilar entry.
  • Regulatory Environment: Increased scrutiny and potential price regulation proposals could cap pricing.
  • Market Penetration: Expansion into new indications and markets can expand total sales volume but may lead to price pressures.

Projected pricing trajectory:

Year Predicted AWP Predicted Retail Price Notes
2024 $8,700 $11,200 Stabilization before biosimilar entry
2025 $8,000 $10,250 Biosimilar launch may reduce originator prices
2026 $7,700 $9,900 Potential further discounts with increased biosimilar competition
2027 $7,500 $9,500 Market stabilization expected

Pricing may decline 10-20% from current levels within five years if biosimilars capture a significant market share.

What Is the Competitive Landscape?

  • Biosimilars: Several biosimilar candidates are in late-stage development, targeting patent expirations for the originator.
  • Patent Protection: The original biologic's patent expires in 2024, opening market access for biosimilars.
  • Market Share: Biosimilars could capture 40-60% of the market within three years of launch, exerting downward pressure on prices.

Regional and Reimbursement Dynamics

  • United States: Prices are influenced by pharmacy benefit managers (PBMs) and Medicare reimbursement policies. The Inflation Reduction Act (IRA) of 2022 may impact pricing and rebates.
  • Europe: Prices are regulated; discounts for government procurement are standard and may range from 15-30% below list price.
  • Asia-Pacific: Growing markets with less regulation but increasing focus on cost containment.

Key Takeaways

  • The drug's market size is approximately $2 billion in the U.S., with steady growth driven by expanded indications.
  • Current prices for a 100 mg vial are around $8,500 (AWP) and $11,000 retail.
  • Future pricing will be influenced by biosimilar competition, regulatory pressures, and market penetration strategies.
  • Biosimilars are expected to enter the market starting 2025, likely decreasing prices by 15-25%.
  • Long-term prices may decline 10-20% over five years as biosimilars gain market share.

FAQs

1. How soon will biosimilars enter the market?
Biosimilar filings are under review, with approval expected in 2024. Commercial availability is anticipated in 2025.

2. Will biosimilars significantly reduce the drug’s price?
Yes. Biosimilars tend to reduce original biologic prices by 15-25%. Such competition could lead to sustained discounts in the coming years.

3. What factors could blunt price declines?
Supply chain constraints, manufacturing complexities, or regulatory challenges could limit biosimilar market penetration, maintaining higher prices.

4. How does the hospital setting influence pricing?
Hospitals often negotiate rebates and discounts, reducing acquisition costs. Payor contracts influence net prices more than sticker prices.

5. Could regulatory policies change price projections?
Yes. Legislation favoring price containment or price caps for high-cost biologics could accelerate price reductions or stabilize prices at lower levels.


Cited Sources:

  1. IQVIA. 2022 Prescription Data.
  2. U.S. FDA. Biosimilar Approvals and Patent Status.
  3. CMS. Medicare Part B Drug Payment Policies.
  4. European Medicines Agency. Biosimilar Market Reports.
  5. Congressional Budget Office. Impact of Biosimilar Competition on Prices.

More… ↓

⤷  Start Trial

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. 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.