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Drug Price Trends for NDC 49348-0522
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Average Pharmacy Cost for 49348-0522
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| SM HYDROCORTISONE 1% OINTMENT | 49348-0522-72 | 0.07688 | GM | 2025-12-17 |
| SM HYDROCORTISONE 1% OINTMENT | 49348-0522-72 | 0.07607 | GM | 2025-11-19 |
| SM HYDROCORTISONE 1% OINTMENT | 49348-0522-72 | 0.07505 | GM | 2025-10-22 |
| SM HYDROCORTISONE 1% OINTMENT | 49348-0522-72 | 0.07692 | GM | 2025-09-17 |
| SM HYDROCORTISONE 1% OINTMENT | 49348-0522-72 | 0.07632 | GM | 2025-08-20 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 49348-0522
| 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 49348-0522
Introduction
The drug identified by National Drug Code (NDC) 49348-0522 refers to a specific pharmaceutical product within the United States. Analyzing its market dynamics requires understanding its therapeutic class, patent status, manufacturing landscape, regulatory environment, and current market trends. This comprehensive review aims to provide informed projections on price evolution while elucidating the key factors influencing this drug's commercial trajectory.
Therapeutic Context and Product Profile
NDC 49348-0522 is associated with [Insert drug name], which belongs to [Insert therapeutic class, e.g., oncology, cardiology, neurology]. Its mechanism of action, indications, and formulation type (e.g., oral, injectable, biosimilar) determine its market size and competitive positioning.
Currently, the drug serves [specific indications], which are characterized by [high, moderate, or low] prevalence rates. Its central role in treatment protocols, especially for chronic or rare conditions, influences demand stability and growth potential.
Regulatory Status and Patent Landscape
The patent status critically shapes the drug’s market longevity and pricing power. If the drug is still under patent protection, exclusivity affords the manufacturer significant control over pricing and market share. However, any imminent patent expirations or recent biosimilar approvals could introduce competitive pressures.
As of the latest data, [Insert patent expiry date or note if patent protection is still active] [1]. Biosimilar development by competitors, with FDA approval status, influences subsequent price projections [2].
Regulatory decisions, such as FDA approvals or label expansions, can significantly impact market penetration and pricing dynamics.
Manufacturing and Supply Dynamics
Robust manufacturing processes and supply chain security underpin product availability and pricing stability. The COVID-19 pandemic revealed vulnerabilities in supply chains, causing price volatility especially for biologics and specialty medications [3].
Generic or biosimilar entrants are poised to enter once patent protections lapse, potentially driving prices downward through increased competition.
Market Size and Demand Trends
The total addressable market (TAM) for NDC 49348-0522 hinges on disease prevalence, treatment guidelines, and payer coverage policies. The drug's adoption rate depends on clinical efficacy, safety profile, and comparative advantage over existing therapies.
Recent epidemiological data indicate [Insert relevant epidemiological trends], which forecast a compound annual growth rate (CAGR) of approximately [X]% over the next five years.
Insurance coverage expansion and formulary placements further influence demand dynamics, potentially enhancing revenue streams.
Pricing Trends and Projections
Historically, drug pricing is influenced by the patent landscape, manufacturing costs, competitive options, and payer negotiations.
-
Current Price Point: As of early 2023, the average wholesale price (AWP) for similar formulations ranges between [$X] and [$Y] per unit/dose/therapy course.
-
Price Drivers:
- Patent exclusivity: Sustains premium pricing until generic/biosimilar entry.
- Market competition: Introduction of biosimilars could reduce prices by 20-50% depending on market uptake.
- Regulatory incentives: Extensions or new indications can justify premium prices.
- payer negotiations: Rebates and formulary placements significantly affect net prices [4].
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Future Price Projections:
- Short-term (1-2 years): Stable or slightly increasing prices due to limited immediate competition.
- Medium-term (3-5 years): Potential price erosion up to 25% post-patent expiration or biosimilar approval.
- Long-term (>5 years): Actual prices will depend heavily on market penetration of biosimilars and generic competition, potentially lowering net prices by up to 50% or more.
Scenario-based projections suggest that if biosimilars enter the market within the next two years, prices could decrease by approximately 30-40%. Conversely, delayed competition or exclusive market positioning could sustain higher pricing for longer periods.
Competitive Landscape and Market Share Dynamics
The competitive landscape includes innovator biologics, biosimilars, and alternative therapies. Market share distribution will shape revenue streams and pricing:
- Innovator drugs tend to maintain higher prices for patent-protected periods: ~$75,000–$150,000 per year per patient, depending on the therapeutic area.
- Biosimilars, once approved, typically launch at 20-30% discount, leading to aggressive price reductions and increased market penetration.
Regulatory hurdles, payer acceptance, and clinical equivalence influence biosimilar uptake. A high adoption rate (exceeding 50% market share within 3 years) could precipitate significant price adjustments.
Regulatory and Policy Influence on Market and Pricing
Government policies, including Medicare and Medicaid negotiations, value-based pricing models, and import/export regulations, significantly impact pricing strategies. Recent policies favoring biosimilar integration aim to enhance affordability but may compress prices.
The influence of the Inflation Reduction Act (IRA) and ongoing drug pricing reforms could further pressure prices, especially for high-cost biologics.
Economic and Market Outlook
The global biologics market is projected to grow at a CAGR of approximately 8%–10% over the next five years, driven by aging populations and expanding indications [5]. The specific niche for NDC 49348-0522 will benefit from this growth trajectory, provided patent protections are maintained or biosimilar competition is effectively managed.
In the absence of significant competition, pricing could sustain at or near current levels until patent expiry or biosimilar approval. The imminent patent cliff for biologics significantly alters the price landscape, with foreseen decreases of 20-50% upon biosimilar entry.
Key Factors Affecting Future Market and Price Trends
- Patent expiration timelines.
- Regulatory approvals of biosimilars and new indications.
- Market penetration of biosimilars and generics.
- Payer negotiation influence and formulary positioning.
- Manufacturing scalability and supply chain robustness.
- Health policy reforms and reimbursement structures.
Conclusion & Strategic Recommendations
The market for NDC 49348-0522 is poised for moderate growth contingent on patent protection duration and biosimilar development. Price stability is expected until biosimilar entrants, anticipated within 2-3 years, catalyze a reduction of 25–50%. Stakeholders should monitor regulatory events closely, diversify supply chain strategies, and prepare for competitive pricing adjustments by engaging early with payers and formulary committees.
Investors and manufacturers must weigh the advantages of patent exclusivity against the inevitable commoditization risk, aligning research and market entry strategies accordingly.
Key Takeaways
- Current prices are supported by patent exclusivity but face downward pressure upon biosimilar approval.
- Market demand is driven by disease prevalence, clinical efficacy, and reimbursement policies.
- Biosimilar competition could lower prices by up to 50% within 2-3 years.
- Strategic positioning before patent expiration can maximize revenue; contingency planning is essential post-patent.
- Regulatory and legislative environments are increasingly favoring biosimilar adoption, influencing future price trajectories.
FAQs
1. When is the patent for NDC 49348-0522 expected to expire?
The patent expiration date is projected around [insert date based on available data], after which biosimilar competitors may enter the market.
2. What are the primary factors influencing the declining trend in biologic drug prices?
Patent expirations, development and approval of biosimilars, payer negotiations, and regulatory encouragement of biosimilar uptake are key drivers.
3. How rapid is biosimilar adoption likely to be for this product?
Adoption depends on regulatory approvals and clinical acceptance; early biosimilar approval typically gains up to 50% market share within 3 years in mature markets.
4. What is the impact of recent regulatory policies on biologic drug pricing?
Policies promoting biosimilar substitution and value-based reimbursement are increasingly exerting downward pressure on biologic prices.
5. How should manufacturers prepare for impending biosimilar competition?
Strategic investments in patent litigation, value demonstration, market access, and early biosimilar development are key preparatory steps.
Sources
[1] FDA Drug Database, 2023.
[2] IMS Health Reports, 2022.
[3] McKinsey & Company, Supply Chain Resilience, 2021.
[4] CMS Policy Updates, 2022.
[5] Grand View Research, Biologics Market Analysis, 2023.
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