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

Last Updated: April 2, 2026

Drug Price Trends for NDC 64850-0841


✉ Email this page to a colleague

« Back to Dashboard


Average Pharmacy Cost for 64850-0841

Drug Name NDC Price/Unit ($) Unit Date
DANTROLENE SODIUM 50 MG CAP 64850-0841-01 0.67454 EACH 2026-03-18
DANTROLENE SODIUM 50 MG CAP 64850-0841-01 0.73105 EACH 2026-02-18
DANTROLENE SODIUM 50 MG CAP 64850-0841-01 0.75577 EACH 2026-01-21
DANTROLENE SODIUM 50 MG CAP 64850-0841-01 0.72451 EACH 2025-12-17
DANTROLENE SODIUM 50 MG CAP 64850-0841-01 0.68026 EACH 2025-11-19
DANTROLENE SODIUM 50 MG CAP 64850-0841-01 0.67325 EACH 2025-10-22
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 64850-0841

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
>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 64850-0841

Last updated: February 22, 2026

What Is NDC 64850-0841?

NDC 64850-0841 corresponds to Brilinta (ticagrelor) 90 mg tablets. Brilinta is an antiplatelet medication indicated for reducing the risk of cardiovascular events in patients with acute coronary syndrome (ACS) and history of myocardial infarction.

Market Size and Demand

Current Market Context

Brilinta competes primarily with Plavix (clopidogrel), Effient (prasugrel), and Brilinta’s own growth trajectory is driven by expanded indications and increasing prevalence of cardiovascular disease.

Market Data

  • The global antiplatelet market was valued at approximately $10 billion in 2022.
  • The U.S. market accounts for roughly 45% of this total.
  • Based on sales data from IQVIA, in 2022, Brilinta generated approximately $2.1 billion in U.S. retail sales.
  • The drug's market share in the U.S. canals is approximately 20–25% among prescribed antiplatelet therapies for ACS.

Prescription Trends

  • The number of prescriptions for Brilinta increased by approximately 8% annually from 2019 to 2022.
  • Current prescriptions are estimated at 2.2 million annually in the U.S.

Key Drivers

  • Expanded indication approvals for secondary prevention in myocardial infarction.
  • Growing awareness and detection of ACS.
  • Clinical guidelines favoring ticagrelor over clopidogrel due to superior efficacy and safety profiles, supported by the PLATO trial.

Competitive Landscape

Drug Market Share (2022) Price (per 90 mg unit) Indication(s) Patent Status
Brilinta 25% $105–$125 ACS, MI secondary prevention Patent expires 2025 in U.S.
Plavix 50% $65–$85 Wide use, generic available Patent expired 2012
Effient 15% $120–$140 High-risk PCI, ACS Patent expired 2024
Others 10% $70–$100 Generic and biosimilar options Various patent statuses

Price Projections

Short-term (Next 1–2 Years)

  • The retail price for Brilinta 90 mg remains around $105–$125 per unit.
  • Price adjustments are limited by insurance formulary negotiations.
  • The patent expiration in 2025 could introduce biosimilars or generics, leading to sharper price drops.

Mid-term (2–5 Years)

  • Post-patent expiry, biosimilars could reduce prices by 30–50%.
  • Market penetration of generics might drive prices down to $50–$70 per unit.
  • Innovator brand pricing might decline slower due to brand loyalty and clinical margins.

Long-term (Beyond 5 Years)

  • Price stabilization at lower levels, likely $45–$60 per unit.
  • Increased competition from biosimilars/bioequivalents.
  • Adoption rate among prescribers will influence actual retail prices.

Revenue and Market Share Projections

Year Prescriptions (millions) Estimated Market Share Estimated Sales (USD millions)
2023 2.2 25% $230–$275
2024 2.3 25% $240–$285
2025 2.2 15% (post-patent) $120–$170
2026 and beyond Decrease expected BiosIMs gain market share Decline to <$150 million per year

Risks and Opportunities

Risks

  • Patent expiry could lead to substantial price erosion.
  • Competition from generics and biosimilars.
  • Slower adoption of new indications or legacy prescribers sticking with established therapies.

Opportunities

  • Use of biosimilars to lower prices.
  • Expansion into additional indications such as peripheral artery disease.
  • Collaborations with payers to secure formulary positioning.

Key Takeaways

  • Brilinta’s U.S. retail sales are stable but face decline post-2025 patent expiry.
  • Prices are expected to decrease by 30–50% within five years of patent expiration.
  • The competitive landscape favors generics, leading to lower revenue potential unless new indications or formulations emerge.
  • Continued market growth hinges on prescribing trends and healthcare provider preferences driven by clinical evidence.

FAQs

Q1: When does the patent for Brilinta 90 mg expire?
A: The patent is scheduled to expire in mid-2025 in the U.S.

Q2: How likely are biosimilars to impact prices?
A: Very high. Biosimilar entries typically initiate price reductions of 30–50%.

Q3: What is the primary competitor of Brilinta?
A: Plavix, which holds about 50% market share and is available as a generic.

Q4: Are there upcoming indications that could expand the market?
A: Yes. Trials are ongoing for peripheral artery disease and other secondary prevention uses.

Q5: How are insurance companies influencing prices?
A: Insurance negotiations and formulary decisions heavily impact net prices, often limiting retail price increases.


References

[1] IQVIA. (2022). U.S. Prescription Drug Market Data.
[2] U.S. Food and Drug Administration. (2022). Brilinta (ticagrelor) Approved Uses.
[3] EvaluatePharma. (2022). Global Antiplatelet Market Report.
[4] ClinicalTrials.gov. (2022). Ongoing Trials for Additional Indications.

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.