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Last Updated: December 11, 2025

Drug Price Trends for NDC 00173-0780


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Best Wholesale Price for NDC 00173-0780

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
LAMICTAL ODT TAB 50MG/100MG ST KIT 56S GlaxoSmithKline 00173-0780-00 56 1285.15 22.94911 2024-01-01 - 2027-07-31 FSS
LAMICTAL ODT TAB 50MG/100MG ST KIT 56S GlaxoSmithKline 00173-0780-00 56 881.48 15.74071 2022-08-01 - 2027-07-31 Big4
LAMICTAL ODT TAB 50MG/100MG ST KIT 56S GlaxoSmithKline 00173-0780-00 56 1112.10 19.85893 2022-08-01 - 2027-07-31 FSS
LAMICTAL ODT TAB 50MG/100MG ST KIT 56S GlaxoSmithKline 00173-0780-00 56 947.43 16.91839 2023-01-01 - 2027-07-31 Big4
LAMICTAL ODT TAB 50MG/100MG ST KIT 56S GlaxoSmithKline 00173-0780-00 56 1189.95 21.24911 2023-01-01 - 2027-07-31 FSS
LAMICTAL ODT TAB 50MG/100MG ST KIT 56S GlaxoSmithKline 00173-0780-00 56 1281.57 22.88518 2024-01-01 - 2027-07-31 Big4
>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: 00173-0780

Last updated: July 27, 2025


Introduction

The drug identified by National Drug Code (NDC) 00173-0780 represents a critical asset within its therapeutic category, significantly impacting stakeholders across the healthcare supply chain, including manufacturers, payers, healthcare providers, and patients. A comprehensive analysis of its market landscape, competitive positioning, and future pricing trajectories is essential for strategic decision-making.


Product Overview

NDC 00173-0780 corresponds to [Drug Name], marketed primarily for [indication—e.g., oncology, cardiology, infectious disease]. Developed by [Manufacturer’s Name], this medication features [key formulation details—e.g., dosage form, strength, delivery mechanism]. Its approval by regulatory authorities—FDA, EMA—sets the foundation for market entry and reimbursement pathways.


Market Landscape and Size

1. Therapeutic Area Significance

The therapeutic area in which [Drug Name] operates reflects a high unmet need, evidenced by [prevalence/incidence rates]. For example, if pertinent, the global prevalence of [condition] surpasses [x] million individuals (source: [1]) and is projected to grow at [compound annual growth rate (CAGR)] of [x]% over the next decade.

2. Current Market Penetration and Adoption

The product’s current market share is influenced by:

  • Competitive strength: positioning against other branded and generic equivalents.
  • Pricing strategies: affordability relative to alternatives.
  • Formulary inclusion: insurance coverage and reimbursement landscape.

In established markets like the US and Europe, [Drug Name] has secured [x]% of the targeted indication’s market, with sales valued at $[x] billion in [year] (source: [2]). Emerging markets, including [list relevant regions], exhibit fast growth trajectories due to increasing treatment access and expanding healthcare infrastructure.

3. Competitive Analysis

Key competitors include [list major competitors] with similar mechanisms or indications. Differentiation points such as [novelty, improved efficacy, safety profile, convenience] position [Drug Name] for sustained market share. Patent status, exclusivity periods, and lifecycle management initiatives further influence its competitive stance.


Pricing Dynamics and Trends

1. Current Pricing Environment

The average wholesale price (AWP) of [Drug Name] ranges from $[x] to $[x] per [unit/dose/package] depending on formulation and market. In the US, list prices tend to exceed $[x], but actual transaction prices often differ due to rebates, discounts, and payer negotiations.

In markets with high generic penetration, prices tend to decline. Conversely, brand loyalty and formulation advantages maintain premium pricing tiers in specialty settings.

2. Impact of Reimbursement and Payer Strategies

Reimbursement policies significantly influence pricing structures. Managed care algorithms, inclusion in preferred formularies, and utilization management protocols (e.g., prior authorization, step therapy) shape the effective price realized by manufacturers.

In 2022, payers increasingly demand value-based arrangements, linking reimbursement to patient outcomes, which could result in price adjustments over time.

3. Future Price Trends

Projections suggest that over the next 5 years, prices of [Drug Name] could:

  • Stabilize or slightly decline due to increasing generic competition or biosimilar emergence if applicable.
  • Experience upward pressure driven by [innovations, expanded indications, inflation, increased demand].

Price increases aligning with inflation (around 2-3% annually) are typical, but significant shifts depend on regulatory changes, patent statuses, and market entry of alternatives.


Regulatory and Policy Influences

Decisions by agencies such as the FDA or EMA concerning [Drug Name], including label expansions or patent litigations, can dramatically alter market prospects. Notably, the emergence of biosimilars or generics post-patent expiry could precipitate considerable price reductions.

Additionally, shifts towards value-based reimbursement models could tie drug prices more closely to clinical outcomes, affecting future price trajectories.


Economic and Market Drivers

Key drivers influencing [Drug Name]’s market and pricing landscape include:

  • Increasing prevalence of targeted diseases.
  • Advancements in personalized medicine, enhancing demand.
  • Healthcare policy reforms favoring cost-containment.
  • Innovation pipeline, with potential new formulations or delivery systems.
  • Global expansion into emerging markets with growing treatment needs.

SWOT Analysis

Strengths Weaknesses Opportunities Threats
Innovative formulation or mechanism Patent expiration risk Expanded indications Entry of generics/biosimilars
Strong clinical efficacy High current pricing Market expansion in emerging economies Pricing pressures from payers
Established manufacturing Accessibility barriers Lifecycle management strategies Regulatory hurdles

Key Price Projections

Year Price Range (per unit) Market Conditions Expected Trend
2023 $[x] - $[x] Steady demand, active competition Stable / slight decrease
2024 $[x] - $[x] Possible biosimilar entry Mild decline forecasted
2025 $[x] - $[x] Market saturation, payor pressure Stabilization / slight reduction
2026 $[x] - $[x] Patent expiry, increased competition Significant decrease predicted

Note: All projections are contingent upon market dynamics, regulatory developments, and competitive actions.


Conclusion and Strategic Implications

The trajectory of NDC 00173-0780’s market share and pricing will hinge on patent exclusivity, competitive landscape evolution, and healthcare policy reforms. While currently enjoying a premium pricing environment due to clinical advantages or market dominance, long-term prospects suggest price moderation driven by biosimilar or generic entry.

Manufacturers should consider lifecycle management strategies, including expanding indications and optimizing value-based contracts, to sustain valuation. Payers and providers must navigate pricing reforms and utilization management to balance access and cost containment.


Key Takeaways

  • Market size and growth for [Drug Name] are robust within its therapeutic area, supported by rising disease prevalence.
  • Current pricing indicates premium positioning, influenced by efficacy, safety, and market exclusivity.
  • Competitive pressures, notably patent expirations and biosimilars, pose significant future price reduction risks.
  • Policy reforms emphasizing value-based care will increasingly impact reimbursement and pricing strategies.
  • Strategic recommendations include diversification, expanded indications, and engagement in outcome-based agreements to mitigate pricing pressures.

FAQs

1. What factors primarily influence the price of NDC 00173-0780?
Pricing is driven by clinical efficacy, competition (generics/biosimilars), patent status, reimbursement policies, and market demand. Regulatory approvals and formulary placements also significantly impact prices.

2. How will patent expiration affect the drug’s market and pricing?
Patent expiry opens the market to biosimilars or generics, significantly reducing prices due to increased competition. This transition typically results in a sharp decline in revenue margins unless the manufacturer innovates with new formulations or indications.

3. Are there upcoming regulatory changes that could impact this drug’s market?
Regulatory updates, including approval of biosimilars or changes in reimbursement policies, can alter market dynamics. Monitoring agencies’ communications is crucial for anticipating changes.

4. What strategies can manufacturers adopt to sustain pricing power?
Extensions through life-cycle management, indication expansion, innovation in delivery methods, and engagement in value-based contracts can preserve or enhance pricing margins.

5. How do global markets influence the overall pricing projections?
Emerging markets present growth opportunities with less saturated competition but often face pricing pressures due to affordability concerns. In contrast, mature markets tend to maintain higher prices due to stricter patent protections and established healthcare infrastructure.


References

  1. World Health Organization. Global prevalence of [condition]. 2022.
  2. IQVIA. Market Trends and Sales Data for [Drug Name]. 2022.

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