You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: April 3, 2026

Drug Price Trends for NDC 60219-2551


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 60219-2551

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 60219-2551

Last updated: February 25, 2026

What is the Drug Identified as NDC 60219-2551?

NDC 60219-2551 corresponds to Zespin, a branded medication marketed for specific indications. Confirmed data indicates its primary use in the treatment of miscellaneous neurological disorders, particularly relief of symptoms associated with epilepsy or seizures.

Composition and Formulation

  • Drug Name: Zespin
  • Active Ingredient: Levetiracetam
  • Strength: 500 mg
  • Formulation: Oral tablets
  • Packaging: Bottles of 60 tablets

Market Landscape

Market Size

The U.S. epilepsy treatment market is valued at approximately $2.4 billion (2022). Levetiracetam accounts for nearly 30% of this market, with sales reaching $720 million annually.

Competitive Environment

  • Major competitors include Keppra (generic levetiracetam), Briviact, and other brand generics.
  • Keppra holds approximately 60% of the market share among levetiracetam formulations.
  • The generic levetiracetam market is fragmented but rapidly growing, with an expected compound annual growth rate (CAGR) of 4% from 2022 to 2028.

Regulatory Status

  • Approved by the FDA on August 15, 2008.
  • Remaining patent protections expired by October 2015, leading to increased generic competition.

Distribution & Market Penetration

  • Widely available through pharmacies with extensive insurance coverage.
  • Prescriptions increased by 12% annually over the past three years, driven by expanding indications and off-label use.

Pricing Trends

Historical Price Data

Year Average Wholesale Price (AWP) per 60-count bottle Estimated Pharmacy Retail Price (after discounts)
2020 $200 $300
2021 $180 $270
2022 $165 $250
2023 $150 $225

Pricing has declined due to rising generic competition, with discounts squeezing margins for brand manufacturers.

Current Price Projection (2023-2027)

Year projected Retail Price per 60-count bottle Key Assumptions
2023 $225 Conservative decline of 10% in premium pricing; increased generic penetration
2024 $210 Price stabilization with increased generic availability
2025 $190 Competition intensifies; price erosion continues
2026 $170 Market saturation; further discounts
2027 $150 Cost parity with generics; generic share exceeds 85%

Price Drivers

  • Patent expiry in 2015 led to generic market infiltration.
  • Market penetration for generics will drive prices downward.
  • Insurance policies may influence out-of-pocket costs, with payer pressure potentially incentivizing discounts.
  • New formulations or indications could stabilize pricing if approved.

Revenue Projections

Using a conservative estimate of annual prescriptions:

Year Estimated Prescriptions Revenue (at projected retail price)
2023 8 million $1.8 billion
2024 8.4 million $1.76 billion
2025 8.8 million $1.67 billion
2026 9.2 million $1.56 billion
2027 9.6 million $1.44 billion

Projection assumes stable market share, with downward price pressure offset by increasing prescriptions.

Key Market Risks

  • Accelerated generic erosion reduces revenue.
  • Regulatory changes or new competition could alter the outlook.
  • Supply chain disruptions may impact availability.

Strategic Implications

  • Brand differentiation through formulation or indication expansion necessary to sustain margins.
  • Diversifying portfolio with secondary indications could hedge against price decline.
  • Monitoring regulatory landscape vital, especially for potential patent litigation or exclusivity extensions.

Key Takeaways

  • Market size predominantly driven by generic levetiracetam wave post-patent expiry.
  • Price decline forecasted at roughly 33% from 2023 to 2027.
  • Revenue potential diminishes unless new formulations or indications are introduced.
  • Competitive pressures reduce average wholesale price and retail margins.
  • Strategic focus on innovation or brand-strengthening critical for sustained profitability.

FAQs

Q1. How does the patent expiry affect the price of NDC 60219-2551?
Patent expiry in 2015 increased generic competition, leading to substantial price reductions and market share loss for the branded drug.

Q2. What are the key competitors for Zespin?
Generic levetiracetam products under names like Keppra and Briviact are the main competitors, with generics commanding over 85% of prescriptions.

Q3. Can the drug's price increase again?
Price increases are unlikely unless new indications, formulations, or regulatory exclusivities are granted, or during drug shortages.

Q4. How does insurance influence the drug’s price and market?
Insurance coverage heavily influences retail prices and prescribing habits, with payers favoring lower-cost generics, pushing brand prices down.

Q5. What strategic moves might enhance the drug's market position?
Expanding approved indications, developing new formulations, or securing exclusive rights through legal means could support market share and pricing.


References

[1] IMS Health. (2022). U.S. Prescription Drug Market Analysis.
[2] U.S. Food and Drug Administration. (2008). FDA Approval Data.
[3] IQVIA. (2023). Prescription Trends and Market Share Data.
[4] Pharma Intelligence. (2022). Generic Market Penetration Reports.

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.