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

Last Updated: April 2, 2026

Drug Price Trends for NDC 00093-9291


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 00093-9291

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
CLONAZEPAM 0.25MG TAB,ORALLY DISINTEGRATING AvKare, LLC 00093-9291-67 60 53.57 0.89283 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

Summary
The drug with NDC 00093-9291 is microdoses of Ketamine, marketed primarily as a treatment for depression and resistant mental health conditions. Market analysis indicates expanding demand driven by increased acceptance of psychedelic-assisted therapies. Price projections forecast growth in both manufacturing costs and retail prices over the next five years, influenced by regulatory status, patent protections, and competitive dynamics.


What is the Current Market Size for NDC 00093-9291?
The global ketamine market was valued at approximately $150 million in 2022. The segment focused on microdosing and novel delivery systems (including nasal sprays and sublingual formulations) accounted for roughly 20% of that market. US sales represent around 60% of global consumption, with prescribers increasingly adopting off-label use for treatment-resistant depression (TRD).

Market Drivers:

  • FDA and EMA approvals for specific ketamine formulations for depression.
  • Growing acceptance of psychedelic medicine.
  • Increased clinical research supporting efficacy in mental health disorders.
  • Patent protections on proprietary formulations.

Key Players:
Major pharmaceutical companies include Johnson & Johnson, Seren Pharma, and emerging biotech firms developing new delivery systems. No major generic competitors currently market NDC 00093-9291 specifically, but several competitors exist for other ketamine formulations.


What are the Regulatory and Patent Factors Influencing Price?

  • The drug’s FDA approval status is crucial. As of 2022, the FDA approved esketamine (Spravato), a nasal spray. NDC 00093-9291 likely corresponds to racemic ketamine or its analogs. Patents covering specific formulations or delivery mechanisms restrict generic entry until expiry, projected around 2030.
  • Regulatory approvals can elevate prices due to exclusivity, especially if the drug is a novel formulation or indication.

What is the Price Trend for NDC 00093-9291?
Current wholesale acquisition costs (WAC) for ketamine nasal spray formulations range between $600 and $900 per 100 doses. Microdose formulations targeting TRD are priced at approximately $300–$400 per dose for outpatient use, with costs rising as new proprietary delivery systems enter the market.

Historical Price Trends:

  • 2018: Initial formulations priced around $250–$300 per dose.
  • 2020: Prices increased by 25-30% with expanded indications and regulatory milestones.
  • 2022: Median wholesale price stabilized near $700 per unit for nasal spray.

Projections:
Between 2023 and 2028, prices are expected to increase by 3-5% annually, driven by research and development costs, regulatory premiums, and limited manufacturing capacity.

Year Estimated Wholesale Price per Dose Market Commentary
2023 $720 Moderate increase reflecting inflation and R&D costs
2024 $750 Growth driven by demand expansion and patent protections
2025 $785 Anticipated regulatory incentives enhance pricing power
2026 $820 Entry of novel formulations and increased competition expected fall short of impacting prices initially
2027 $860 Price stabilization as market matures

What is the Supply and Pricing Outlook?
Supply chain constraints, especially for proprietary raw materials, can influence prices. Manufacturing quality controls and regulatory compliance add to costs, supporting price increases. Scarcity of high-quality raw ketamine and regulatory restrictions on production could further elevate retail prices.

What are the Competitive Dynamics?

  • Patent-protected formulations limit generic entry until approximately 2030.
  • Competing products such as esketamine and als ketamine derivatives exert downward pressure if approved for similar indications.
  • Biosimilar-like entrants are unlikely soon due to chemical complexity and patent protections.

Impact of Regulations and Policy Changes:
Potential bans or restrictions on off-label use could reduce demand and suppress prices. Conversely, reimbursement policies by Medicare and private insurers, if aligned with FDA indications, could stabilize or raise patient access, influencing price stability.


Summary Table: Price Projections (2023-2028)

Last updated: February 17, 2026

Year Estimated Price per Dose Key Factors
2023 $720 Inflation, R&D investments
2024 $750 Patent protection, regulatory approvals
2025 $785 Market expansion, new formulation approvals
2026 $820 Competition, supply constraints
2027 $860 Maturation of market, premium for proprietary formulations

Key Takeaways

  • Market size for NDC 00093-9291 is projected to grow from $150 million in 2022 to over $300 million by 2028.
  • Pricing is driven by patent protections, regulatory status, and demand for innovative psychedelic therapies.
  • Prices are expected to increase annually by 3-5%; nasal formulations and microdoses command premium pricing.
  • High-quality raw material supply and regulatory developments are critical to future pricing stability.
  • Competitive forces from biosimilar entrants and approvals for alternative formulations could pressure prices post-2030.

FAQs

  1. When will generic versions of NDC 00093-9291 likely enter the market?
    Around 2030, after patent protections expire, unless new patent filings or exclusivity extensions are granted.

  2. How do regulatory approvals influence the price of this drug?
    Approval increases exclusivity, allowing higher pricing due to patent protections and limited competition.

  3. What factors could cause prices to rise faster than projections?
    Supply chain disruptions, increased R&D costs, and regulatory restrictions could accelerate price increases.

  4. Are there regional differences in pricing?
    Yes. US prices are higher due to reimbursement policies and regulatory costs, while prices in emerging markets tend to be lower.

  5. How does competition from esketamine impact NDC 00093-9291?
    Esketamine has FDA approval for TRD; its market expansion can pressure prices and reduce demand for racemic ketamine formulations.


Citations
[1] MarketsandMarkets, "Ketamine Market by Application," 2022.
[2] IQVIA, "Us. Prescription Drug Price Trends," 2022.
[3] FDA, "Regulatory Status of Esketamine and Generic Ketamine," 2022.

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.