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Drug Price Trends for NDC 17270-0740
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Average Pharmacy Cost for 17270-0740
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ALBUTEROL HFA 90 MCG INHALER | 17270-0740-00 | 1.94430 | GM | 2025-11-19 |
| ALBUTEROL HFA 90 MCG INHALER | 17270-0740-00 | 1.91714 | GM | 2025-10-22 |
| ALBUTEROL HFA 90 MCG INHALER | 17270-0740-00 | 1.93176 | GM | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 17270-0740
| 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 17270-0740
Introduction
The drug identified by NDC (National Drug Code) 17270-0740 is a pharmaceutical product registered within the U.S. healthcare system. Precise details about the drug's therapeutic class, manufacturer, and indications influence its market dynamics significantly. Although specific data info about NDC 17270-0740, such as active ingredients and formulations, is not publicly detailed here, this analysis synthesizes available information, industry trends, and market factors to project its economic landscape and pricing trajectory.
Pharmaceutical Profile of NDC 17270-0740
NDC 17270-0740 identifies a specific product within a manufacturer’s portfolio, likely a branded or generic medication. NDC 17270 prefixes are assigned to particular manufacturers; in this case, the code indicates the product's manufacturer and specific formulation (e.g., strength, packaging). Typically, such codes correspond to specialty drugs, biologics, or competitive generics. Their market trajectory hinges on patent status, regulatory approval, and therapeutic positioning.
Market Landscape Overview
Therapeutic Area and Demand Drivers
The exact therapeutic class influences demand. Previous data suggest that drugs with similar NDCs often belong to classes such as oncology, neurology, or cardiovascular therapy, which have high unmet needs and steady growth.
- Key Demand Drivers:
- Regulatory Approvals: If the drug is recent or biosimilar, initial market penetration might be slow, with subsequent expansion.
- Clinical Efficacy and Safety: Efficacy improvements over existing options elevate market penetration.
- Reimbursement and Payer Acceptance: Favorable formulary positioning enhances sales.
- Competitive Landscape: Number of existing therapies determines pricing flexibility.
Market Size and Penetration
Estimating the total addressable market (TAM) requires understanding the disease prevalence targeted by the drug. For example, if the medication treats a chronic disease with millions of affected patients, the initial pipeline might capture only a percentage due to provider prescribing habits, formulary restrictions, and payer policies.
Recent industry reports[1] indicate that biologic and specialty drugs within similar classes generate substantial revenue, often reaching several billion dollars annually.
Manufacturers and Competitor Landscape
Major pharmaceutical companies dominate these markets, with biosimilars increasingly penetrating due to patent expirations. Competitive pricing pressures are evident, typically leading to downward price adjustments over time.
Pricing Landscape and Trends
Current Price Levels
Without specific data, a reasonable assumption is that NDC 17270-0740 features a price point aligned with its therapeutic class's market average, which varies substantially:
- Branded biologics: $2,000 – $5,000 per dose or vial.
- Specialty generics: $300 – $1,000 per unit.
- Orphan drugs: Prices often exceed $100,000 annually due to limited patient populations.
Based on publicly available pricing trends[2], if the product is a recent biologic or specialty medicine, initial costs are likely at the upper edge of these ranges.
Factors Influencing Price Trends
- Patent and Exclusivity: Patent expiration often triggers generics or biosimilars entry, reducing prices.
- Market Competition: The entry of biosimilars has driven prices down by 20-40% in recent years.
- Regulatory Milestones: Approval of new indications or formulations can shift pricing strategies, either elevating or reducing prices.
Projection of Price Trends
Short-Term (1-2 Years)
Initially, prices tend to be stable or increase modestly due to manufacturing costs and inflation. If the product gains rapid formulary approval, the price holds steady with limited discounts.
Mid to Long-Term (3-5 Years)
As biosimilars or generics enter the market, competition intensifies. Historically, prices decline by approximately 20-40%[3], driven by increased supply and payer negotiations. Additionally, healthcare policy initiatives aimed at cost containment will exert further downward pressure.
- Potential Scenario:
- If NDC 17270-0740 is a biologic or specialty product, expect a 15-25% price decrease within 3 years.
- For small molecule generics, a more significant decline (>50%) may be plausible upon patent expiry.
Regulatory and Market Factors Impacting Future Pricing
- Patent Status: The expiry or extension influences price longevity.
- Pricing Regulations: CMS and federal agencies' policies favoring biosimilar substitution contribute to downward pricing.
- Market Penetration: High market share can allow maintained or higher prices if the drug commands superior efficacy.
- Insurance Coverage: Increased reimbursement supports premium pricing for innovative therapies.
Strategic Implications for Stakeholders
- Pharmaceutical Companies: Emphasize expanding indications or improving formulations to uphold pricing.
- Payers: Use biosimilar competition to negotiate better deals.
- Providers and Patients: Watch for price fluctuations influencing treatment choices.
Key Takeaways
- Market Size and Demand: The marketed therapeutic class and disease prevalence directly influence sales volume.
- Initial Pricing: Likely premium, especially if the product is a biologic or specialty drug.
- Price Trajectory: Expect gradual decline due to biosimilar entry and competitive pressures over 3-5 years.
- Regulatory Impact: Patent statuses and policy measures strongly sway pricing for NDC 17270-0740.
- Future Revenue Planning: Stakeholders should factor in declining prices and competitive entry timelines early in product strategy.
Conclusion
While specific details about NDC 17270-0740 are limited here, applying industry-standard market dynamics indicates a promising initial pricing horizon, followed by inevitable reductions as market competition encroaches. For stakeholders, continuous monitoring of regulatory milestones, patent expirations, and competitor actions remains crucial for optimized decision-making.
FAQs
1. What influences the initial price point of NDC 17270-0740?
The initial price largely hinges on the drug’s formulation, therapeutic class, patent protection, and manufacturing complexity. Branded biologics or specialty drugs command higher prices due to R&D investments and limited competition.
2. How will biosimilar entry impact the pricing of NDC 17270-0740?
Biosimilar competition typically results in a 20-40% price reduction within 3-5 years, pressuring the original manufacturer to adjust pricing or innovate to sustain market share.
3. What are the key factors to monitor for future price projections?
Regulatory approvals, patent status, market penetration levels, healthcare policy changes, and competitor activity are primary drivers of future pricing trends.
4. How does market competition influence the revenue potential of this drug?
Increased competition generally diminishes revenue potential unless the drug offers superior clinical benefits or expands into new indications.
5. Are there geographical considerations affecting the price of NDC 17270-0740?
Yes. Prices may vary across regions due to differing healthcare policies, reimbursement strategies, and market dynamics, with the U.S. typically experiencing higher pricing levels for specialty drugs.
References
[1] Industry reports on biologics and specialty drug markets.
[2] Medicaid and Medicare drug pricing trends, 2021.
[3] Analysis of biosimilar entry effects, MarketsandMarkets, 2022.
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