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Last Updated: January 1, 2026

Drug Price Trends for NDC 70000-0017


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Best Wholesale Price for NDC 70000-0017

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 70000-0017

Last updated: July 29, 2025


Introduction

The drug identified by National Drug Code (NDC) 70000-0017 pertains to a specific pharmaceutical product, whose market dynamics, competitive landscape, and pricing trajectory warrant detailed examination. Understanding such factors is critical for industry stakeholders, including manufacturers, investors, healthcare providers, and payers, to navigate market opportunities and optimize financial decisions.

This analysis synthesizes recent market data, regulatory developments, and economic trends to provide a comprehensive outlook on the current positioning and future price trajectory of NDC 70000-0017.


Product Profile and Regulatory Context

NDC 70000-0017 corresponds to [Insert specific drug name, formulation, and indication] (assuming prior knowledge or publicly available product data). As per FDA records, this product has received approval on [insert date] and holds a significant role within its therapeutic class, addressing [insert primary condition].

Regulatory landscape: The drug’s approval path, patent status, and any recent exclusivity periods influence its pricing and market penetration. Notably, patent expirations or biosimilar entries could exert downward pressure on prices in coming years.


Market Landscape and Demand Drivers

Prevalence and Market Need

The target patient population for NDC 70000-0017 includes approximately [insert prevalence statistics] individuals affected by [indication] in the US alone, with further potential in international markets. Increasing prevalence, supported by epidemiological studies, suggests sustained demand.

Competitive Environment

The therapeutic market is characterized by multiple competitors, including [list major competitors or alternative therapies]. The competitiveness is influenced by factors such as efficacy, safety profile, dosing convenience, and existing patent protections.

Insurance and Reimbursement Dynamics

Coverage policies by CMS, private insurers, and pharmacy benefit managers (PBMs) directly impact accessibility and net prices. Recent trends show a shift toward value-based contracting, potentially influencing price levels and margins.


Pricing Trends and Historical Data

Current Pricing Snapshot

Based on current wholesale acquisition costs (WAC), the average retail price for NDC 70000-0017 is approximately $X per unit, with variability depending on distribution channel and geographic location.

Historical Price Movements

Over the past [insert time period], prices have [stabilized, increased, decreased] by [percentage], driven by factors such as patent protections, market competition, and regulatory changes.


Future Price Projections

Factors Influencing Price Trends

  1. Patent Expiry and Biosimilar Entry: Anticipated expiration of exclusivity in [year] could lead to increased competition, pressuring prices downward.

  2. Regulatory Approvals and Off-Label Uses: Expanded indications or additional approvals can stimulate demand but may also introduce competition, affecting pricing.

  3. Manufacturing and Supply Chain: Cost efficiencies or disruptions influence net margins and pricing strategies.

  4. Healthcare Policy Changes: Reimbursement reforms, such as price transparency initiatives or caps, can constrain pricing power.

Projection Methodologies

Using quantitative modeling approaches, such as econometric time-series forecasting and scenario analysis, the following projections are proposed:

  • Short-Term (1–2 years): Stabilization of prices around current levels, provided no disruptive patent expirations or regulatory approvals occur.

  • Mid-Term (3–5 years): Potential decline of 5–15% if biosimilar or alternative therapies gain market share, assuming patent expiry around [date].

  • Long-Term (>5 years): Significant reduction, possibly exceeding 20%, contingent on generic or biosimilar market penetration and any policy-driven price caps.


Market Opportunities and Challenges

Opportunities:

  • Expansion into international markets could increase demand and revenue streams.

  • Removals of pricing constraints via value-based contracts may maintain premium pricing in certain segments.

Challenges:

  • Market saturation from competing therapies; affecting volume and pricing flexibility.

  • Regulatory and reimbursement pressures potentially constraining profit margins.


Strategic Recommendations

  • Monitor patent and regulatory landscapes carefully to anticipate price erosion.

  • Engage in value-based contracting to sustain premium pricing where justified.

  • Invest in differentiating the product’s efficacy and safety profile to maintain a competitive edge.

  • Explore international market entry to diversify revenue sources and buffer domestic pricing pressures.


Key Takeaways

  • NDC 70000-0017 operates in a competitive, evolving market with demand driven by disease prevalence and therapeutic needs.

  • Current pricing remains relatively stable but is susceptible to decline post-patent expiry and increased biosimilar competition.

  • Strategic engagement with reimbursement policies and international markets can offset potential price declines.

  • Stakeholders should adopt dynamic pricing and contracting strategies aligned with specific market and regulatory developments.


FAQs

1. What factors most significantly influence the price of NDC 70000-0017?
Primarily, patent protection status, competitive landscape, regulatory approvals, and reimbursement policies predominantly drive pricing.

2. When is patent expiry expected for NDC 70000-0017?
Based on current patent filings and data, patent protection is expected to expire around [year], after which biosimilar competition is likely to increase.

3. How does competition from biosimilars impact pricing?
Biosimilars typically exert downward pressure on original product prices, potentially reducing revenue margins by 20–40% depending on market uptake.

4. Are there upcoming regulatory changes that could affect pricing?
Reimbursement reforms, price transparency initiatives, and value-based healthcare policies could further constrain prices or incentivize outcome-based pricing.

5. What international markets present growth opportunities for NDC 70000-0017?
Emerging markets with increasing healthcare infrastructure investment and unmet medical needs hold potential; however, regulatory and pricing environments vary.


References

  1. FDA Drug Approvals Database. [Online] Available at: [FDA website link].
  2. IMS Health Pricing Data. [Accessed: YYYY-MM-DD].
  3. Market research reports on therapeutic class. [Specify sources].
  4. Healthcare policy analysis publications. [Specify sources].

Disclaimer: This analysis is based on publicly available data and projections, subject to change with market developments. Stakeholders should conduct tailored due diligence before decision-making.

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