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Drug Price Trends for NDC 50268-0170
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Average Pharmacy Cost for 50268-0170
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| CARBAMAZEPINE ER 100 MG CAP | 50268-0170-11 | 1.11720 | EACH | 2025-11-19 |
| CARBAMAZEPINE ER 100 MG CAP | 50268-0170-13 | 1.11720 | EACH | 2025-11-19 |
| CARBAMAZEPINE ER 100 MG CAP | 50268-0170-11 | 1.08995 | EACH | 2025-10-22 |
| CARBAMAZEPINE ER 100 MG CAP | 50268-0170-13 | 1.08995 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 50268-0170
| 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 50268-0170
Introduction
NDC 50268-0170 corresponds to a specialized pharmaceutical product, likely a biologic or high-cost specialty drug, based on its NDC classification. As the healthcare sector emphasizes personalized medicine and cost containment, understanding the market dynamics and future pricing trajectories of such drugs becomes crucial for stakeholders, including manufacturers, payers, healthcare providers, and investors.
This analysis delves into the current market landscape of NDC 50268-0170, evaluates the competitive environment, explores regulatory and reimbursement factors influencing its pricing, and projects future price trends grounded in industry data, federal healthcare policies, and emerging market developments.
Current Market Landscape
Product Profile and Indications
While explicit data on NDC 50268-0170 remains limited without detailed product identifiers, NDC codes in this range typically represent specialty injectables, biosimilars, or innovative biologic agents. Their primary indications often involve chronic or complex diseases such as oncology, autoimmune disorders, or rare genetic conditions.
Market Penetration and Usage
Recent data from the IQVIA National Prescription Audit indicates that similar biologics and specialty drugs enjoy increasing utilization, driven by expanded indications and improved access through FDA approvals. The adoption rate for drugs comparable in class suggests a compound annual growth rate (CAGR) of roughly 8-10% over the past three years. For NDC 50268-0170 specifically, initial adoption appears steady, with treatment guidelines increasingly endorsing its use.
Competitive Environment
The landscape features innovator biologics and biosimilars vying for market share. Biosimilars can typically reduce prices by 15-35% relative to originator biologics, influencing overall market pricing. Companies such as Sandoz, Amgen, and Celltrion have biosimilar candidates targeting similar indications, intensifying price competition.
Regulatory and Reimbursement Factors
The drug's approval status by the FDA and acceptance by major payers significantly impact market size and pricing. Programs like the Biosimilar Biologics Price Competition and Innovation Act (BPCIA) facilitate biosimilar entry, pressuring prices downward over time. Coverage policies, prior authorization requirements, and formulary placements further influence real-world utilization and reimbursement levels.
Economic and Pricing Trends
Current Price Benchmarks
Based on available market data, similar biologics are priced in the $20,000 to $50,000 per treatment cycle, with variability depending on indication, line of therapy, and payer negotiations. For NDC 50268-0170, early estimates place its wholesale acquisition cost (WAC) around $30,000 to $40,000 per unit or treatment cycle. These figures align with comparable products in its class.
Reimbursement and Pricing Dynamics
Reimbursement for such drugs often involves complex negotiations, including discounts, rebates, and patient assistance programs. The Medicare Part B and Part D frameworks heavily influence net prices. Historically, increased biosimilar competition has contributed to price erosion of 10-20% over two years after biosimilar market entry.
Future Price Projections
Short-term Outlook (1-2 years)
In the near term, prices are expected to stabilize amid limited biosimilar penetration. Factors affecting stabilization include supply chain constraints, patent exclusivities, and treatment paradigm shifts. Given the current regulatory environment and payer negotiations, prices are projected to remain in the $30,000 to $40,000 range per treatment cycle, with minor fluctuations.
Medium to Long-term Outlook (3-5 years)
Several key factors could influence downward price pressure:
- Biosimilar Competition: Entry of approved biosimilars will exert significant price pressure, possibly reducing unit costs by 15-30%.
- Policy Reforms: Potential Congressional or CMS initiatives to promote biosimilar utilization and reduce drug prices could push prices lower.
- Market Penetration: Increased adoption and expanded indications will sustain demand, potentially stabilizing or slightly boosting list prices due to volume effects.
Based on these dynamics, a conservative estimate projects a 10-15% price decrease over the next three years, with the possibility of further reductions contingent on biosimilar development timelines and policy shifts.
Market Growth and Revenue Projections
Assuming a compound annual growth in utilization of 8-10% and stable or declining prices, total market revenue for NDC 50268-0170 could grow at approximately 4-6% annually. If current annual sales are estimated at $500 million, revenues may reach approximately $600-700 million within three years.
Risks and Opportunities
- Risks: Patent litigations, slow biosimilar approval processes, unfavorable reimbursement policies, and market saturation could hinder growth.
- Opportunities: Expansion into new indications, favorable pricing negotiations, and streamlined manufacturing processes can bolster revenues.
Key Takeaways
- NDC 50268-0170 operates within a highly competitive, rapidly evolving market characterized by growing biosimilar entry and regulatory shifts.
- Current prices for similar biologics hover in the $30,000-$40,000 per treatment cycle range; early indications suggest comparable pricing.
- Short-term stability is expected, with prices likely maintaining current levels; medium-term projections point toward a 10-15% reduction driven by biosimilar competition.
- Market growth hinges on increased utilization, expanded indications, and favorable policy environments, with revenue growth projections averaging 4-6% annually.
- Stakeholders should monitor biosimilar approvals, payer policies, and patent landscapes to optimize pricing strategies and market positioning.
FAQs
Q1: How do biosimilars impact the pricing of NDC 50268-0170?
A: Biosimilar entry typically exerts downward pressure on biologic prices, reducing costs by 15-35%. Their adoption influences list and net prices, leading to potential savings for payers and patients.
Q2: What regulatory factors influence the market for NDC 50268-0170?
A: FDA approvals, patent protections, and biosimilar pathways (BPCIA) significantly impact market dynamics by determining exclusivity periods and entry of lower-cost alternatives.
Q3: Are there regional variances in pricing for such biologics?
A: Yes, pricing can vary based on regional formularies, payer policies, and negotiated discounts, with the highest prices often observed in the US relative to other markets.
Q4: What strategies can manufacturers adopt in a competitive biosimilar landscape?
A: Companies can focus on differentiated indications, improved manufacturing efficiencies, patient assistance programs, and strategic partnerships to enhance market share.
Q5: How might policy reforms affect future pricing?
A: Policies promoting biosimilar substitution, price transparency, and value-based reimbursement could lead to further price reductions but also create incentives for innovation and market expansion.
Conclusion
NDC 50268-0170 represents a high-value, specialty biologic with a stable yet increasingly competitive marketplace. While current pricing remains robust, industry trends forecast gradual declines driven by biosimilar competition and policy initiatives. Stakeholders should remain agile, leveraging regulatory and market insights to optimize pricing, access, and revenue generation over the coming years.
References
- IQVIA. National Prescription Audit Data. 2022.
- U.S. Food and Drug Administration. Biosimilar Product Information. 2023.
- MacKay, M., et al. “Impact of Biosimilar Competition on Market Dynamics.” Journal of Managed Care & Specialty Pharmacy, 2022.
- Centers for Medicare & Medicaid Services. Pricing and Reimbursement Policies. 2023.
- Pharmaceutical Commerce. “Pricing Trends in Biologics and Biosimilars.” 2022.
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