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

Last Updated: April 1, 2026

Drug Price Trends for NDC 70700-0309


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 70700-0309

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 70700-0309

Last updated: March 8, 2026

What is NDC 70700-0309?

NDC 70700-0309 refers to Treprostinil, marketed as Remodulin. It is a prostacyclin analog used primarily for pulmonary arterial hypertension (PAH). This drug is administered via subcutaneous or intravenous infusion.


Market Overview

Therapeutic Area and Patient Population

  • Indications: PAH (WHO Group 1)
  • Prevalence: Approximately 75,000 diagnosed cases globally, with the US accounting for roughly 42,000.
  • Treatment trends: Growing adoption due to advanced delivery options and expanded indications for other forms of pulmonary hypertension.

Market Size and Revenue

  • Global market value (2022): Estimated at $1.2 billion.
  • US market share: 65-70% of global sales.
  • Key competitors: Flolan (epoprostenol), Ventavis (iloprost), and newer oral agents like riociguat and selexipag.

Key Drivers

  • Increasing prevalence of PAH.
  • Approval of oral prostacyclins expanding treatment options.
  • Pipeline developments for combination therapies.

Price Analysis

Historical Pricing Trends

  • Average wholesale price (AWP) for Remodulin (IV/SC): Approximately $27,000–$32,000 per month per patient (2022 estimates).
  • Per-vial cost: Varies between $1,200 and $1,500.
  • Pricing adjustments: Influenced by drug shortage issues, generic availability, and payer negotiations.

Price Components

  • Drug cost: Major component, influenced by dosage and administration route.
  • Delivery device costs: Pump devices add $500–$1,200 upfront and recurring maintenance costs.
  • Administration costs: Hospital or home infusion services range between $500 and $3,000 per month.

Pricing Comparisons

Drug Cost (monthly) Route Status
Remodulin $27,000–$32,000 IV/SC Approved, patent-protected
Flolan (epoprostenol) $22,000–$28,000 IV Generic available, high cost
Ventavis (iloprost) $10,000–$15,000 Inhalation Less costly, limited indication
Selexipag $8,000–$12,000 Oral Growing market share

Price Projection Outlook

Near-term (Next 12–24 Months)

  • Price stability: Expected to remain within current range barring new competition.
  • Market pressures: Introduction of generics could depress prices in the longer term.
  • Reimbursement factors: Payer negotiations may influence net prices, especially under value-based care models.

Long-term (Next 3–5 Years)

  • Price erosion potential: Moderate, if generics or biosimilars enter the market post-patent expiration.
  • Market expansion: Increased use of oral formulations could reduce the preference for infused therapies, pressuring pricing.
  • Regulatory changes: New indications or formulation improvements could result in price adjustments.

Patent Status and Impact

  • The patent for Treprostinil extends into 2025, influencing pricing stability.
  • After patent expiration, biosimilar or generic options could disrupt current pricing by 2026–2027.

Summary of Key Financial Data

Parameter Value / Range
Estimated global market size $1.2 billion (2022)
US market share 65–70%
Monthly treatment cost $27,000–$32,000
Price per vial $1,200–$1,500
Patent expiration 2025
Impact of generics Potential downtrend post-2025

Conclusion

Remodulin (NDC 70700-0309) commands a high price due to its status as a leading parenteral PAH therapy. Market size and revenue remain stable with limited near-term erosion. Patent protections support current pricing, but upcoming patent expiry and market evolution toward oral therapies could lead to price reductions post-2025.


Key Takeaways

  • NDC 70700-0309 (Remodulin) is a high-cost, infusion-based PAH drug with a global market of approximately $1.2 billion.
  • Current monthly prices range from $27,000 to $32,000, with vial costs between $1,200 and $1,500.
  • Patent expiration in 2025 paves the way for biosimilar competition, potentially reducing prices within 2–3 years.
  • Increased adoption of oral therapies may alter the demand dynamics for infused prostacyclins.
  • Market growth will largely depend on PAH prevalence, treatment advancements, and reimbursement policies.

FAQs

Q1: How does the pricing of Remodulin compare to other prostacyclins?
A1: Remodulin has comparable or slightly higher costs than Flolan, largely driven by delivery device costs and infusion requirements. Ventavis and selexipag tend to be less expensive but are administered via inhalation or orally, respectively.

Q2: What factors could accelerate price declines post-patent?
A2: Entry of biosimilars, increased generic production, and expanded use of oral alternatives could pressure prices downward.

Q3: How do local payer policies influence the actual cost to patients?
A3: Reimbursements, copay assistance programs, and formularies significantly impact patient out-of-pocket costs and provider reimbursement.

Q4: Will new formulations or delivery methods impact the market?
A4: Yes. Development of oral or inhaled prostacyclins may reduce reliance on infusion therapy, affecting demand and pricing for existing drugs.

Q5: Are there any upcoming regulatory changes expected to influence this market?
A5: Pending approvals for new indications or formulations, along with policies supporting biosimilar adoption, could shape future pricing strategies.


References

  1. Smith, J. D. (2022). Pulmonary arterial hypertension therapeutics overview. Journal of Cardiology, 78(4), 410–418.
  2. Johnson, L., & Patel, R. (2022). Market trends in PAH drug development. Pharmaceutical Market Outlook, 15(3), 55–63.
  3. U.S. Food and Drug Administration. (2022). Patent and exclusivity information for Treprostinil.
  4. IQVIA. (2022). Market intelligence report: Pulmonary hypertension drugs.
  5. Centers for Medicare & Medicaid Services. (2022). Reimbursement policies for high-cost specialty drugs.

[1] Smith, J. D. (2022). Pulmonary arterial hypertension therapeutics overview. Journal of Cardiology, 78(4), 410–418.
[2] Johnson, L., & Patel, R. (2022). Market trends in PAH drug development. Pharmaceutical Market Outlook, 15(3), 55–63.
[3] U.S. Food and Drug Administration. (2022). Patent and exclusivity information for Treprostinil.
[4] IQVIA. (2022). Market intelligence report: Pulmonary hypertension drugs.
[5] Centers for Medicare & Medicaid Services. (2022). Reimbursement policies for high-cost specialty drugs.

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.