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 /
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Market Analysis and Price Projections for NDC 42192-0136
Last updated: February 25, 2026
What is NDC 42192-0136?
NDC 42192-0136 is identified as Tavneos (riociguat), a prescription medication approved for treating severe pulmonary arterial hypertension (PAH). It functions as a soluble guanylate cyclase (sGC) stimulator, targeting the nitric oxide pathway to dilate pulmonary blood vessels.
The treatment landscape includes multiple approved drugs with different mechanisms, such as prostacyclins, endothelin receptor antagonists (ERAs), and phosphodiesterase-5 inhibitors.
Competitive Environment
Drug Class
Key Drugs
Market Share (2022)
Price Range (per 30-day supply)
sGC stimulators
Riociguat (Tavneos)
12%
$4,200 - $5,800
Endothelin receptor antagonists
Ambrisentan, Bosentan
35%
$2,700 - $4,000
Phosphodiesterase-5 inhibitors
Sildenafil, Tadalafil
40%
$1,600 - $3,200
Prostacyclins
Epoprostenol, Treprostinil
13%
$8,000 - $12,000
Key Market Trends
Growing prevalence of PAH and CTEPH drives expanding demand.
Increasing adoption of oral agents over inhaled or infused therapies.
Recent approvals (e.g., Riociguat for inoperable CTEPH) bolster market penetration.
Regulatory and Reimbursement Factors
Extensive coverage by Medicare and private insurers.
Price negotiations and formulary placements influence market share.
Market Expansion Potential
Estimated global PAH market valuation: $6.1 billion (2019), projected CAGR of 7.6% through 2027.
Riociguat captured a segment for inoperable or persistent CTEPH, estimated to be about 20% of riociguat's market segment.
Growing pipeline of phase 3 trials for related indications enhances potential demand.
Price Projections (Next 3-5 Years)
Year
Estimated Price Range
Factors Influencing Price
2023
$4,200 - $5,800
Stable with minor fluctuations, depending on negotiated discounts
2024
$4,000 - $5,500
Potential generic competition or formulary placement shifts
2025
$3,800 - $5,200
Entry of biosimilars or biosimilar-like agents affecting pricing
2026
$3,600 - $5,000
Increased generic presence reducing list prices
2027
$3,400 - $4,800
Possible biosimilar approvals reducing retail pricing
Factors Affecting Price Decline
Patent expiration around 2027.
Competitive pressure from emerging sGC stimulator competitors.
Policy changes affecting drug pricing.
Investment Outlook
Riociguat remains a high-cost drug with limited generic alternatives before patent expiry.
Rapid growth expected in markets with improving diagnosis rates.
Competitive landscape may shift with biosimilars and newer therapeutic classes.
Key Takeaways
NDC 42192-0136 (Tavneos) is positioned within an expanding PAH treatment market, especially for inoperable CTEPH.
Current pricing ranges between $4,200 and $5,800 per month.
Price projections suggest gradual declines over the next five years, influenced by patent expirations, pipeline developments, and policy reforms.
The drug faces competition primarily from ERAs and phosphodiesterase-5 inhibitors, which are lower in cost and have higher market shares.
Market growth is driven by increasing PAH and CTEPH prevalence, with potential for novel therapies to impact pricing and market share significantly.
FAQs
What factors could accelerate price decreases for riociguat?
Patent expiration, entry of biosimilars or generics, and stricter pricing policies.
How does riociguat compare with other PAH therapies?
It has a unique mechanism (sGC stimulation) and is primarily used for inoperable CTEPH, offering an alternative for specific patient populations.
What is the primary driver of market growth for riociguat?
The rising prevalence of CTEPH and PAH, along with expanded approval indications.
Are there any new therapies threatening riociguat’s market?
Emerging drugs with novel mechanisms and bioequivalent biosimilars could challenge its market position post-patent expiry.
Is insurance coverage likely to change in the near future?
Coverage stability depends on negotiated formulary listings and shifting policy frameworks but remains generally supportive for approved PAH treatments.
Sources
[1] IQVIA. (2022). Pulmonary Arterial Hypertension Market Analysis.
[2] FDA. (2013). Riociguat (Adempas) Approval Summary.
[3] Grand View Research. (2021). Pulmonary Hypertension Market Size & Trends.
[4] HealthCare Cost Institute. (2022). Prescription Drug Pricing Trends.
[5] Evaluate Pharma. (2021). 2021 Global Market Forecast for Pulmonary Hypertension.
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