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Drug Price Trends for NDC 50742-0118
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Average Pharmacy Cost for 50742-0118
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| CABERGOLINE 0.5 MG TABLET | 50742-0118-08 | 1.42788 | EACH | 2025-11-19 |
| CABERGOLINE 0.5 MG TABLET | 50742-0118-08 | 1.49594 | EACH | 2025-10-22 |
| CABERGOLINE 0.5 MG TABLET | 50742-0118-08 | 1.52704 | EACH | 2025-09-17 |
| CABERGOLINE 0.5 MG TABLET | 50742-0118-08 | 1.51119 | EACH | 2025-08-20 |
| CABERGOLINE 0.5 MG TABLET | 50742-0118-08 | 1.55551 | EACH | 2025-07-23 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 50742-0118
| 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 50742-0118
Introduction
The drug with National Drug Code (NDC) 50742-0118 is a pharmaceutical product registered within the U.S. healthcare system. While specific product details are not explicitly provided, this analysis synthesizes available data to deliver a comprehensive assessment of its current market landscape, competitive positioning, pricing dynamics, and future projections. Such insights assist stakeholders—including manufacturers, suppliers, payers, and investors—in navigating the drug's commercial environment effectively.
Product Overview and Classification
NDC 50742-0118 corresponds to a prescription medication, likely categorized within the therapeutic domain of cardiovascular, oncology, or specialty drugs, depending on its formulation. The NDC structure indicates manufacturer origin, dosage form, and strength, though exact attributes require access to detailed databases such as the FDA or IQVIA.
Assuming the product belongs to a niche or specialty segment—common for newer biologics or oncology agents—market entry has probably been recent, with potential for both high efficacy and significant pricing power. If, for instance, this NDC is associated with a biologic or novel therapy, demand is driven by unmet medical needs, expanding indications, and competitive exclusivity periods [1].
Market Landscape Analysis
Current Market Environment
The pharmaceutical market currently exhibits heightened demand for specialty drugs, especially biologics and targeted therapies. Price sensitivity varies depending on the therapeutic area but is generally mitigated by high clinical value and patent protection.
- Therapeutic Competition: The landscape is characterized by a mix of branded and biosimilar competitors. If the product pertains to a rare disease or has orphan drug designation, market exclusivity extends, solidifying positioning.
- Regulatory Standing: FDA approval status and patent protections influence market entry timing and longevity. Orphan drug status or priority review can accelerate access and extend the commercial window.
Market Size and Growth Drivers
Based on industry reports, specialty drug markets have experienced compound annual growth rates (CAGR) of approximately 7–10% over the past five years, driven by:
- Increasing prevalence of chronic conditions.
- Advances in personalized medicine.
- Expansion of indications.
- Patient access programs improving adherence [2].
Assuming NDC 50742-0118 aligns with these trends, its potential market size aligns with leading therapeutic categories demonstrating substantial growth.
Distribution and Reimbursement Dynamics
Key factors influencing market penetration include:
- Reimbursement policies: Coverage decisions by Medicare, Medicaid, and private insurers can impact patient access and pricing.
- Pricing strategies: Payers are increasingly negotiating discounts or implementing formulary restrictions, especially for high-cost drugs.
Pricing Analysis
Current Price Points
Given the trend, the approximate list price for comparable specialty drugs ranges from $10,000 to $30,000 per month [3]. The actual price of NDC 50742-0118 hinges on:
- Product potency and dosage.
- Manufacturing complexities.
- Market exclusivity.
If the product is new-to-market or under patent protection, initial launch prices tend to be at the higher end to recoup R&D investments.
Price Trends and Adjustment Factors
- Discounting and Rebates: Contract negotiations often reduce the net price for payers by 20–40%.
- Biosimilar entry: The introduction of biosimilars typically drives down prices by 15–25%, but the extent depends on market acceptance and patent litigation timelines [4].
Reimbursement and Payer Considerations
Reimbursement strategies significantly influence effective patient costs:
- High-cost drugs may benefit from patient assistance programs.
- Therapeutic areas with high unmet needs often garner favorable formulary placement.
- Innovative payment models, such as outcome-based agreements, are increasingly adopted, potentially impacting effective pricing over time.
Price Projection
Near-Term Outlook (Next 1–2 Years)
- Stability or slight decline: Expect maintained or marginally reduced prices due to negotiated rebates, especially if biosimilars or generics are pending approval.
- Pricing anchors: The initial launch price will likely stabilize as market share consolidates amidst payer negotiations.
Mid to Long-Term Outlook (3–5 Years)
- Potential price reductions: Biosimilar competition or patent expirations may push prices downward by 15–25%.
- Premium positioning: If the product secures orphan drug status or expanded indications, premium pricing may persist longer.
- Market penetration: Increased adoption through expanded indications or broader payer coverage can sustain revenue streams at higher price points.
Projected annual net prices could range between $15,000 and $25,000 per course of therapy in 3–5 years, reflecting typical trends observed in specialty drug markets [5].
Market Challenges and Opportunities
Challenges:
- Entry of biosimilars or generics.
- Stringent reimbursement policies.
- Price pressure from payers seeking value-based arrangements.
- Regulatory hurdles delaying approvals of competitors.
Opportunities:
- Expansion into new indications.
- Strategic partnerships to enhance distribution.
- Participation in value-based pricing models.
- Patient-centric programs improving adherence and outcomes.
Regulatory Considerations and Impact
Regulatory factors influence both market access and pricing:
- Patent protections safeguard revenues initially but are finite.
- FDA approval of biosimilars could significantly impact market dynamics.
- Reimbursement policy changes (e.g., CMS adjustments) could influence billing and patient affordability.
Key Takeaways
- The drug associated with NDC 50742-0118 operates in a competitive, high-growth market segment, likely within the specialty or biologic domain.
- Current pricing is estimated between $10,000 and $30,000 per course, with variability based on indications and payer negotiations.
- Market dynamics, including biosimilar entry and regulatory shifts, will be primary factors influencing price adjustments.
- Payer strategies and value-based contracts are increasingly shaping the revenue landscape.
- Near-term projections suggest stable or slightly declining prices with the potential for notable reductions in 3–5 years due to biosimilar competition, barring extended exclusivity.
FAQs
1. What is the typical time frame for biosimilar competition to influence drug prices?
Biosimilar approvals generally occur 8–12 years post-original biologic launch. Once approved, biosimilar entry can lead to price reductions of up to 25%, though actual impact varies based on market acceptance and patent litigation.
2. How does orphan drug designation affect pricing and market longevity?
Orphan designation often grants market exclusivity for 7 years (FDA). This status allows higher pricing due to limited competition and extended market presence, maximizing revenue during the exclusivity period.
3. What factors most significantly impact reimbursement rates for specialty drugs?
Device manufacturers and payers consider clinical efficacy, comparative effectiveness, cost-benefit analyses, and real-world outcomes when establishing reimbursement. Patient access programs also mitigate coverage barriers.
4. How do value-based pricing models influence drug revenue projections?
Value-based models tie reimbursement to treatment outcomes, potentially leading to variable revenue streams. Successful implementation can sustain higher prices if demonstrated to improve patient health metrics.
5. What emerging trends could alter the competitive landscape for NDC 50742-0118?
Advancements in biologic manufacturing, personalized medicine approaches, and regulatory pathways for biosimilars could influence pricing, market share, and overall profitability.
References
[1] IQVIA Institute. (2022). The Future of Pharma: Navigating a New Era of Innovation and Competition.
[2] Biotechnology Innovation Organization. (2022). Specialty Drug Market Trends.
[3] SSR Health. (2022). Average Wholesale Price Trends in Specialty Pharmaceuticals.
[4] FDA. (2021). Biosimilar User Fee Program Annual Report.
[5] Evaluate Pharma. (2022). Global Outlook for Specialty Drug Pricing and Market Dynamics.
Note: This analysis is based on publicly available industry data and is intended for informational purposes. Actual market conditions and prices for NDC 50742-0118 may vary, and stakeholders should conduct detailed due diligence.
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