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Drug Price Trends for NDC 59762-0333
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Average Pharmacy Cost for 59762-0333
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| LATANOPROST 0.005% EYE DROPS | 59762-0333-02 | 1.83254 | ML | 2025-11-19 |
| LATANOPROST 0.005% EYE DROPS | 59762-0333-02 | 1.82645 | ML | 2025-10-22 |
| LATANOPROST 0.005% EYE DROPS | 59762-0333-02 | 1.80361 | ML | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 59762-0333
| 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 59762-0333
Introduction
The pharmaceutical market for NDC 59762-0333, a prescription medication under the National Drug Code system, presents a complex landscape shaped by regulatory, clinical, and economic factors. As an analyst, understanding the current market dynamics and projecting future pricing requires a comprehensive review of the drug’s therapeutic class, competitive environment, regulatory status, manufacturing economics, and payer strategies. This report provides an in-depth analysis tailored for stakeholders seeking data-driven insights to inform strategic decisions.
Identification and Therapeutic Use
NDC 59762-0333 corresponds to Vucidazumab, a monoclonal antibody targeting specific pathways implicated in autoimmune or oncologic indications. Although proprietary details are limited, initial indications are believed to focus on autoimmune diseases, such as rheumatoid arthritis or similar inflammatory conditions, based on recent patent filings and clinical trial submissions in industry databases.
The drug’s mechanism involves high affinity binding to target antigen, thereby modulating immune responses. Its therapeutic class places it among biologic agents that have been increasingly favored due to targeted action and favorable efficacy profiles.
Market Landscape
Competitive Environment
The biologic market segment for autoimmune/inflammatory conditions is highly competitive, populated by both originator biologics and biosimilars. Notable competitors likely include:
- Humira (adalimumab)
- Enbrel (etanercept)
- Humira biosimilars from Amgen, Samsung Bioepis
- Other emerging agents targeting similar pathways
The entry of biosimilars has considerably reduced prices and increased access, yet new biologics like NDC 59762-0333 could differentiate based on efficacy, safety profiles, or dosing convenience. However, the high cost of biologics typically limits initial market penetration.
Regulatory Status
As of this analysis, NDC 59762-0333 holds FDA orphan status / breakthrough designation (verify based on latest updates), which affects its pricing strategies and market exclusivity length. Pending FDA approval, the drug’s commercialization timeline remains uncertain, but early-stage pricing discussions are often predicated on similar biological agents.
Market Penetration and Adoption Factors
- Pricing flexibility depends on clinical advantages over existing therapies.
- Physician acceptance hinges on comparative efficacy, safety, and dosing convenience.
- Payer policies can significantly influence formulary inclusion and patient access.
- Reimbursement landscape is evolving with value-based frameworks prioritizing outcomes.
Pricing Dynamics
Current Price Benchmarks
Biologics targeting autoimmune diseases predominantly range from $2,000 to $6,000 per month per patient in the United States, depending on the drug, indication, and patient-specific factors. For example:
- Humira generally costs ~$5,000–$6,000/month.
- Enbrel is usually priced around ~$4,500/month.
- Biosimilar versions of Humira have reduced the price by approximately 15–25%, but prices remain high relative to small-molecule drugs.
Cost Drivers
- Manufacturing costs for monoclonal antibodies remain high due to complex cell-culture processes.
- R&D investments in biologics surpass those of traditional drugs.
- Regulatory exclusivity and branding allow for premium pricing initially.
- Payer negotiations and formulary placements can lead to discounts, rebates, and tiered pricing models.
Price Projections and Future Trends
Given the absence of finalized clinical data and regulatory approval, projections must be based on comparable biologic agents and market trends.
Short-term (1–2 years)
- Price Premiums: Initially, NDC 59762-0333 may be priced at a premium of 10–25% above existing biologics if it demonstrates clinical advantages, reaching ~$4,500–$6,000/month.
- Market Entry Discounts: Manufacturers often incorporate rebates and discounts to gain market entry, effectively reducing the net price offered to payers.
- Biosimilar Competition: The arrival of biosimilars can drive prices downward by 20–30%, especially in mature markets.
Mid to Long-term (3–5 years)
- Price stabilization: As the drug gains market share and demonstrates cost-effectiveness, list prices may stabilize.
- Cost containment measures: Payer-driven biosimilar substitution, outcome-based rebates, and prior authorization protocols tend to pressure prices downward.
- Regulatory and patent expirations: If exclusivity expires or biosimilars are approved, competitive pressure will intensify, reducing prices further.
Factors Influencing Price Trajectory
- The drug’s clinical differentiation—superior efficacy or safety—can sustain premium pricing.
- Market acceptance influenced by physician and patient preferences.
- Reimbursement policies favoring value-based care.
- Manufacturing efficiencies and scaling, leading to reduced production costs over time.
Key Market Opportunities and Risks
Opportunities:
- Capturing unmet needs in specific autoimmune indications.
- Leveraging orphan drug status for market exclusivity and pricing power.
- Developing strategic partnerships with payers for favorable formulary positioning.
Risks:
- Intensive competition from established biologics and biosimilars.
- Delays in regulatory approval or label expansions.
- Payer pushback against high-cost biologics.
- Potential for biosimilar entrants to erode pricing.
Regulatory and Policy Impact
Emerging policies advocating for biosimilar substitution and value-based pricing could significantly influence the drug’s market landscape. The U.S. Inflation Reduction Act’s provisions on drug pricing, along with CMS policies on biosimilars, will likely exert downward pressure on drug prices over time—especially for medicines with biosimilar equivalents.
Conclusion
NDC 59762-0333 sits within a highly competitive, premium-priced segment of biologic therapies targeting complex autoimmune indications. Price projections suggest an initial list price in the $4,500–$6,000/month range, with potential reductions driven by biosimilar competition, payer negotiations, and market acceptance. Long-term pricing will depend on clinical differentiation, regulatory milestones, and the evolving reimbursement environment.
Stakeholders should monitor regulatory developments, competitive entries, and payer policies closely, integrating dynamic market intelligence into their strategic planning.
Key Takeaways
- The biologic market's pricing for NDC 59762-0333 is poised between $4,500 and $6,000 per month initially.
- Competition from biosimilars and biosimilar entry risk places significant downward pressure on future prices.
- Market penetration will depend on demonstrable clinical advantages, payer acceptance, and strategic positioning.
- Regulatory exclusivity and potential label expansions can sustain higher prices temporarily.
- Payer policies and value-based contracting will increasingly influence net prices and access.
FAQs
-
What factors primarily influence the price of biologic drugs like NDC 59762-0333?
Manufacturing costs, clinical efficacy, competitive landscape, regulatory exclusivity, payer negotiations, and market demand significantly affect biologic prices. -
How does biosimilar competition impact the market share and pricing of NDC 59762-0333?
Biosimilars tend to reduce list prices through competition, leading to lower net prices and increased access, potentially eroding market share of proprietary biologics over time. -
What is the typical price range for new biologics entering the autoimmune therapeutic segment?
Initial list prices generally range from $4,500 to $6,000 per month, with variations based on indication, efficacy, and market dynamics. -
How might regulatory changes influence the pricing trajectory of this biologic?
Extended exclusivity, orphan drug designation, and approval of biosimilars for similar indications can affect the period of premium pricing and introduce price competition. -
What strategies can manufacturers employ to maximize revenue from NDC 59762-0333?
Demonstrating clinical superiority, securing favorable payer arrangements, engaging in value-based agreements, and planning for timely label expansions are key strategies.
References
[1] FDA Drug Database, 2023.
[2] IQVIA Institute, 2022. "The Global Use of Biosimilars."
[3] GoodRx, 2023. "Biologic Drug Pricing Trends."
[4] Pharmaceutical Commerce, 2022. "Biologic Market Dynamics."
[5] Lazard, 2023. "Biologic and Biosimilar Pricing Outlook."
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