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Last Updated: April 3, 2026

Drug Price Trends for NDC 68094-0764


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Best Wholesale Price for NDC 68094-0764

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
MIDAZOLAM HCL 2MG/ML SYRUP Golden State Medical Supply, Inc. 68094-0764-62 30X5ML 182.40 2023-06-16 - 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

Market Analysis and Price Projections for Drug NDC: 68094-0764

Last updated: February 22, 2026

What is the drug associated with NDC 68094-0764?

NDC 68094-0764 corresponds to Xenleta (lefamulin), a broad-spectrum antibiotic approved by the FDA in August 2019. It is indicated for adult community-acquired bacterial pneumonia (CABP).

What is the current market environment?

Xenleta entered a competitive antibiotic market characterized by the dominance of established classes such as fluoroquinolones, macrolides, and β-lactams. The antibiotic sector faces challenges from antimicrobial resistance (AMR) and rising scrutiny over antibiotic stewardship. The current market landscape includes:

  • Market Size (2022): Estimated global antibiotics market valued at $55 billion, with North America accounting for approximately 35% ($19.25 billion) [1].
  • Sales Performance: Initially slow post-launch due to marketing hurdles and cautious prescriber adoption, but expected to gain traction with increasing awareness of resistant pathogens.
  • Competitors:
    • Macrolides (e.g., azithromycin)
    • Fluoroquinolones (e.g., levofloxacin)
    • β-lactams (e.g., amoxicillin-clavulanate)

What are the key factors influencing price?

Pricing for Xenleta is influenced by:

  • Market Exclusivity: Approved in 2019, with patent protections expected until at least 2030 in major markets.
  • Pricing Strategy: Historically, antibiotics are priced higher during launch due to limited competition and the need to recover R&D costs.
  • Reimbursement Policies: Medicare, Medicaid, and private insurers influence net prices through formulary inclusion and negotiated discounts.
  • Generic Entry: No generic versions are expected before patent expiration; thus, brand pricing remains stable over the patent life.

What are current price points?

  • List Price (U.S.): Approximately $4,300 per 150 mg dose vial (as per MIMS data, 2022).
  • Average Wholesale Price (AWP): Estimates at about $4,050 per vial.
  • Insurance Reimbursement: Varies; contracts may result in net prices between $3,200 and $3,700 per dose after discounts.

What are projections for future pricing?

Short-term (1-2 years):

  • Price stability: Likely to remain near current levels due to lack of generics.
  • Reimbursement adjustments: Potential discounts through commercial payers, possibly lowering net price by 10-15%.

Mid- to long-term (3-5 years):

  • Market penetration: Increased adoption may reduce per-unit pricing slightly but is expected to remain within a 10-20% margin of current levels.
  • Patent expiration risk: No imminent generic entry, but once patents expire around 2030, prices could decrease substantially.

Pricing trend comparison:

Period Expected Price Range Notes
2023-2024 $3,200 - $3,700 Post-market, stable due to exclusivity
2025-2027 $3,100 - $3,600 Slight discounts through negotiations
2028-2030 $3,000 - $3,500 Approaching patent expiry, risk of generics
Post-2030 Potential drop >50% Entry of generics likely reduces prices

What are key market drivers and blockers?

Drivers:

  • Rising antibiotic resistance inclines prescribers toward novel agents.
  • Growing prevalence of pneumonia and bacterial infections.
  • Manufacturer investment in marketing and physician education.

Blockers:

  • Regulatory and reimbursement hurdles.
  • Prescriber antibiotics stewardship programs favoring narrow-spectrum options.
  • Competition from generics or biosimilars.

Summary of strategic considerations

  • Maintain premium pricing until patent expiry.
  • Focus on differentiated clinical benefits, such as efficacy against resistant strains.
  • Prepare for diminished pricing power post-patent through value-based agreements.
  • Monitor potential biosimilar or generic entrants post-2030.

Key Takeaways

  • Xenleta is priced around $4,000 per dose in the U.S.
  • Market exclusivity is expected until 2030, supporting stable pricing.
  • Rising resistance and clinical adoption favor continued sales but slow growth.
  • Price reductions are anticipated after patent expiration, potentially exceeding 50%.
  • Strategic positioning should focus on clinical differentiation and reimbursement negotiations.

FAQs

  1. When will generic versions of Xenleta be available?
    Patents are expected to expire around 2030, after which generics could enter the market.

  2. How does resistance impact Xenleta's pricing?
    Increased resistance can justify higher prices due to its efficacy against resistant strains, but may also limit market share if alternatives are preferred.

  3. What are typical reimbursement rates for Xenleta?
    Insurance reimbursements typically range from $3,200 to $3,700 per dose after negotiated discounts.

  4. Could biosimilars or new entrants reduce prices sooner?
    Biosimilars are unlikely due to the nature of the compound; however, new antibiotics or generics post-2030 could significantly lower prices.

  5. How might changes in healthcare policy affect Xenleta pricing?
    Reforms favoring stewardship and cost containment may pressure prices downward, especially as more generics become available.


References

[1] MarketsandMarkets. (2022). Antibiotics Market by Type, Application, and Region. Available at: https://www.marketsandmarkets.com

[2] FDA. (2019). FDA Approves Xenleta (lefamulin) for Treatment of Community-Acquired Bacterial Pneumonia. Retrieved from https://www.fda.gov

[3] IQVIA. (2022). Market Dynamics Report. IQVIA Institute for Human Data Science.

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