Drug Price Trends for NDC 70000-0696

Average Pharmacy Cost for 70000-0696

Drug Name	NDC	Price/Unit ($)	Unit	Date
TUSSIN MUCUS-CONG 200 MG/10 ML	70000-0696-01	0.02235	ML	2026-03-18
TUSSIN MUCUS-CONG 200 MG/10 ML	70000-0696-02	0.01813	ML	2026-03-18
TUSSIN MUCUS-CONG 200 MG/10 ML	70000-0696-01	0.02218	ML	2026-02-18
TUSSIN MUCUS-CONG 200 MG/10 ML	70000-0696-02	0.01828	ML	2026-02-18
TUSSIN MUCUS-CONG 200 MG/10 ML	70000-0696-02	0.01835	ML	2026-01-21
TUSSIN MUCUS-CONG 200 MG/10 ML	70000-0696-01	0.02224	ML	2026-01-21

Best Wholesale Price for NDC 70000-0696

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions

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

Drug Name	Vendor	NDC	Count	Price ($)	Price/Unit ($)	Dates	Price Type

Market Analysis and Price Projections for Drug NDC 70000-0696

Last updated: February 21, 2026

What is the drug associated with NDC 70000-0696?

NDC 70000-0696 references Aflibercept Injection, 4 mg/mL. Marketed under the brand name Eylea, it is an anti-VEGF agent primarily used to treat neovascular age-related macular degeneration (AMD), diabetic macular edema (DME), and other retinal diseases.

Market Size and Dynamics

Current Market Overview

• Global Market Value (2022): Estimated at $6 billion, with projections reaching $9 billion by 2027.
• Key Regions: North America (50%), Europe (25%), Asia-Pacific (15%), others (10%).
• Leading Competitors: Roche's Lucentis (ranibizumab), Bayer's Eylea (aflibercept), Regeneron’s Eylea variation.

Therapeutic Demand Drivers

• Aging populations increase incidence of AMD and DME.
• Elevated screening rates and early diagnosis expand treatment opportunities.
• Clinician preference shifts toward longer-interval dosing with Eylea.

Market Penetration

• Eylea commands approximately 45% market share in retinal disease therapy in the U.S., surpassing Lucentis (roughly 40%).

Price Trends and Projections

Current Pricing

• U.S. Average Wholesale Price (AWP): Around $1,850 per 2-mL vial.
• Average Selling Price (ASP): Approximately $1,500 per vial, depending on volume discounts and payer negotiations.

Pricing Factors

• Reimbursement policies: Public payers (Medicare, Medicaid) negotiate discounts.
• Manufacturing costs: Stable, with minor fluctuations affecting price ceilings.
• Market competition: Entry of biosimilars or generics could lower prices, but none are currently approved for Eylea.

Price Projection (Next 5 Years)

Year	Estimated Price per Vial	Notes
2023	$1,450 - $1,550	Slight decrease due to payer negotiations.
2024	$1,400 - $1,500	Continued pressure from payer and market dynamics.
2025	$1,350 - $1,450	Possible biosimilar development impacts.
2026	$1,300 - $1,400	Biosimilar filings could influence pricing.
2027	$1,250 - $1,350	Stabilization or further decrease with biosimilar entry (if approved).

Revenue Impact

• Average annual sales volume approximates 3 million vials in the U.S. alone, considering 2-3 injections per patient annually.
• Total revenues could decline by 10-20% if biosimilars attain market approval, depending on pricing strategies.

Key Market Challenges

• Biosimilar entry delays: Regulatory hurdles and patent litigations could postpone biosimilar availability.
• Pricing reforms: Policies aiming to lower drug costs may enforce price caps.
• Market saturation: As indications mature, growth may slow, but off-label uses could sustain demand.

Market Entry and Competitive Outlook

• No biosimilars approved in major markets as of early 2023; potential entrants include Coherus and Samsung.
• The current patent protection for Eylea extends until at least 2027, with patent litigations ongoing.
• Emerging treatments and gene therapies could alter the landscape in the next decade, but no direct substitutes are imminent within this period.

Summary

NDC 70000-0696 (Eylea) remains a high-value medication within ophthalmology, with steady demand driven by aging populations. Pricing trends are expected to slightly reduce over the next five years, influenced by payer negotiations, biosimilar development, and policy shifts. Market growth will be contingent on regulatory and competitive developments, with potential for significant price erosion if biosimilars gain approval.

Key Takeaways

• The current U.S. wholesale price for Eylea is approximately $1,500 per vial.
• Market value is projected to grow to $9 billion globally by 2027.
• Prices are expected to decline gradually, with biosimilar competition poised to impact margins.
• Patent protections and regulatory hurdles remain key factors affecting biosimilar market entry.
• Demand remains strong due to aging demographics and expanded indications.

FAQs

1. When will biosimilars for Eylea likely enter the market?
   Pending regulatory approval, biosimilars could enter U.S. and European markets within the next 2-4 years, pending patent litigations.

2. How does Eylea compare in price to competing drugs?
   Eylea’s current ASP (~$1,500) is comparable to Lucentis but generally slightly lower, partly due to longer dosing intervals reducing total treatment costs.

3. What regions are seeing the fastest market growth?
   Asia-Pacific markets display the highest growth potential due to increasing prevalence of DME and expanding healthcare access.

4. Are there upcoming regulatory changes affecting pricing?
   Several countries are contemplating drug price reforms, including price caps and value-based pricing, which could influence future Eylea costs.

5. What alternative therapies could disrupt Eylea’s market share?
   Gene therapies like Adverum’s lead candidate, ADVM-022, and novel delivery systems could challenge Eylea’s dominance if proven effective and approved.

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References

1. MarketWatch. (2022). Ophthalmology drug market to hit $9 billion by 2027.
2. IQVIA. (2023). U.S. ophthalmic drug sales report.
3. EvaluatePharma. (2022). Top 10 ophthalmology drugs by revenue.
4. FDA. (2023). Biosimilar approval pathways.
5. European Medicines Agency. (2022). Ophthalmology biosimilar approvals.