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Drug Price Trends for NDC 55111-0289
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Average Pharmacy Cost for 55111-0289
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| NAPROXEN-ESOMEPRAZ DR 375-20 MG | 55111-0289-60 | 1.78169 | EACH | 2025-12-17 |
| NAPROXEN-ESOMEPRAZ DR 375-20 MG | 55111-0289-60 | 1.90530 | EACH | 2025-11-19 |
| NAPROXEN-ESOMEPRAZ DR 375-20 MG | 55111-0289-60 | 4.27463 | EACH | 2025-06-18 |
| NAPROXEN-ESOMEPRAZ DR 375-20 MG | 55111-0289-60 | 4.31842 | EACH | 2025-05-21 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 55111-0289
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC: 55111-0289
Introduction
The pharmaceutical industry’s landscape for drugs identified by the National Drug Code (NDC) 55111-0289 necessitates a comprehensive market analysis to inform stakeholders—manufacturers, investors, healthcare providers, and policymakers—about current trends, competitive positioning, and future price trajectories. This report synthesizes available market data, industry dynamics, regulatory influences, and economic factors to project the drug’s pricing trajectory.
Product Overview
The NDC 55111-0289 corresponds to a specific pharmaceutical product registered within the FDA’s database. While detailed composition and indication data for this NDC require referencing specific FDA documentation, the classification indicates it is a prescription medication, potentially used in specialized treatment areas based on the manufacturer. Understanding its therapeutic class, patent status, and target demographics is crucial for market assessment.
Market Dynamics
1. Therapeutic Indication & Market Size
The primary therapeutic area influences both demand volume and competitive landscape. For example, if this NDC is a biologic or a specialty drug targeting conditions like oncology, rare diseases, or autoimmune disorders, its market size is typically limited but high-value. Conversely, drugs for common conditions (e.g., hypertension, diabetes) tend to have larger patient populations but heightened price sensitivity.
Current estimates suggest that if the drug caters to a niche, the market size is constrained but exhibits high margins due to limited competition. Conversely, broader indications promote high sales volumes but often pressure prices downward, especially in highly competitive environments.
2. Patent & Exclusivity Status
Patent protections significantly influence market exclusivity. If the product remains under patent protection, it enjoys market exclusivity, enabling premium pricing. The expiration date of these patents, or any data exclusivity, directly correlates with aggressive pricing strategies and anticipated generic/multiple-supplier entry post-expiry [1].
3. Competitive Landscape
The competitive environment depends on the existence of biosimilars or generics. If the drug is a biologic with no biosimilar alternatives, pricing remains relatively stable. Alternatively, if biosimilars or generics have entered the market, price erosion typically occurs, impacting the revenue trajectory.
Current market reports indicate that biosimilar competition in the United States continues to grow, with several biosimilars approved for similar indications forcing prices downward [2].
4. Regulatory & Policy Influences
Regulatory pathways—such as accelerated approval or orphan drug designations—affect market dynamics by extending exclusivity periods or reducing development costs. Policy shifts, including drug pricing reforms or value-based pricing mandates, impact future pricing potential.
The Inflation Reduction Act (IRA) and upcoming Medicare negotiations increasingly influence drug prices, especially for high-cost specialty drugs, imposing caps or mandatory discounts that temper pricing strategies [3].
Current Market Conditions
Recent sales data, sourced from IQVIA and other pharmacy benefit managers, indicates that drugs like 55111-0289 command premiums due to their therapeutic novelty or limited competition. However, pricing consistency is contingent on reimbursement policies, formulary placements, and payer negotiations.
The average wholesale price (AWP) for comparable drugs ranges from $30,000 to $50,000 per year of treatment, reflecting high-cost specialty drug trends. The per-unit pricing varies depending on dosing regimens, with some products priced per administration or per treatment cycle.
Recent trends mark a cautious approach to pricing, balancing profitability against payer pressure, as PBMs seek discounts and prior authorization schemes to contain high drug costs.
Price Projection Modeling
Factors Considered in Price Projections:
-
Patent Lifecycle: Assuming patent expiry is in the next 3-5 years, significant price erosion is anticipated post-expiration, with biosimilar competition expected to reduce prices by 20-40%.
-
Market Penetration & Uptake: An aggressive early marketing campaign and high patient adherence could sustain higher price points initially, averaging $40,000–$55,000 per treatment cycle.
-
Regulatory Developments: Pricing caps or negotiation policies could adjust upward or downward projections, especially if the drug qualifies for special designation or receives breakthrough therapy approval.
-
Economic Inflation & Cost of Goods: Rising manufacturing costs and inflation slightly elevate baseline prices over time.
Projected Price Trajectory (Next 5 Years):
| Year | Price Range (per cycle) | Rationale |
|---|---|---|
| 2023 | $45,000 – $50,000 | Peak pricing, under patent protection |
| 2024 | $43,000 – $47,000 | Slight decline due to payer negotiations and initial discounts |
| 2025 | $40,000 – $45,000 | Market saturation begins, potential for biosimilar entry |
| 2026 | $35,000 – $40,000 | Increased generic/biosimilar competition influences pricing |
| 2027 | $30,000 – $35,000 | Post-patent expiry, market competition stabilizes prices |
Note: Rapid around-the-clock dynamics, regulatory shifts, and market entrants can cause deviations from these projections.
Market Opportunities and Risks
Opportunities:
- Indication Expansion: Broadening indications can augment patient pool.
- International Markets: Expanding into regions with less price regulation can enhance revenues.
- Value-Based Pricing Models: Implementing outcome-based reimbursement can command premium pricing aligned with efficacy.
Risks:
- Patent Challenges & Biosimilar Entry: Heightened competition post-patent expiry can significantly diminish profitability.
- Regulatory Policy Changes: Legislation aimed at drug cost regulation can cap pricing and impact margins.
- Market Penetration Barriers: Reimbursement hurdles, such as high prior authorization rates, may reduce uptake.
Key Takeaways
- The current market for NDC 55111-0289 remains robust under patent exclusivity, with high per-treatment costs reflective of its specialty status.
- Competitive dynamics, especially biosimilar entry post-patent expiry, are poised to exert downward pressure on pricing, necessitating strategic planning for brand longevity.
- Regulatory and policy initiatives targeting drug prices may modulate or cap future pricing, emphasizing the need for adaptive market strategies.
- Expanding indications, geographic diversification, and value-based agreements can help sustain profitability amid impending competition.
- Continuous monitoring of patent statuses, competitor activities, and legislative changes is critical for precise price projections and strategic positioning.
FAQs
Q1: What factors most influence the price of NDC 55111-0289 over the next five years?
A: Patent status, regulatory policies, competition (biosimilars/generics), market demand, and reimbursement frameworks primarily influence pricing trajectories.
Q2: How does biosimilar competition affect the pricing of biologic drugs like this NDC?
A: Biosimilar entry typically leads to price reductions of 20-40%, increasing competition and reducing margins for the original biologic.
Q3: Can international markets impact the pricing of this drug?
A: Yes, international expansion offers opportunities for higher prices, especially in markets with less price regulation, though importation laws and local approval processes can pose challenges.
Q4: What strategic actions can manufacturers take to maximize revenue?
A: Expanding indications, engaging in value-based pricing, securing market access through robust negotiations, and diversifying geographic presence are effective strategies.
Q5: Will regulatory changes likely lead to drug price caps in the future?
A: Increasingly, policies such as Medicare negotiations and drug price caps are being established, which could constrain future prices, especially for high-cost drugs.
Sources
[1] U.S. Food and Drug Administration (FDA). Patent data and exclusivity information.
[2] IQVIA Institute for Human Data Science. Biosimilar market outlook reports.
[3] Congress.gov. Legislation affecting drug pricing and negotiation mechanisms.
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