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Drug Price Trends for NDC 62135-0271
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Average Pharmacy Cost for 62135-0271
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| RAMIPRIL 1.25 MG CAPSULE | 62135-0271-01 | 0.09673 | EACH | 2025-11-19 |
| RAMIPRIL 1.25 MG CAPSULE | 62135-0271-30 | 0.09673 | EACH | 2025-11-19 |
| RAMIPRIL 1.25 MG CAPSULE | 62135-0271-01 | 0.09514 | EACH | 2025-10-22 |
| RAMIPRIL 1.25 MG CAPSULE | 62135-0271-30 | 0.09514 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62135-0271
| 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 62135-0271
Introduction
The drug identified by NDC 62135-0271 pertains to a specific pharmaceutical product registered within the United States' National Drug Code (NDC) system. Precise identification of this drug encompasses understanding its therapeutic class, formulation, manufacturer, and approved indications. This analysis aims to provide a detailed market landscape, competitive positioning, pricing trajectory, and future projections—serving as a strategic guide for stakeholders including pharmaceutical companies, investors, healthcare providers, and policy-makers.
Product Profile and Regulatory Status
The NDC code 62135-0271 is associated with [Insert drug name, e.g., 'Xyzal (levomilnacipran)], a [antidepressant/antiviral/oncology agent, etc.] indicated for [list approved indications]. Manufactured by [manufacturer's name], the drug has received FDA approval on [date], with [or without] exclusivity rights, spanning a typical 5-7 year exclusivity period depending on patent protection or orphan designation.
Recent regulatory filings suggest [any label updates, supplemental approvals, or patent litigations], influencing current market dynamics. The drug's patent expiry, expected around [date], critically shapes future market presence and generic entry timelines.
Market Landscape Overview
Current Market Size and Segmentation
Based on industry reports and proprietary data, the global market for [therapeutic class] was valued at approximately $X billion in [year], with the U.S. accounting for roughly Y% of this volume (~$Z billion). The drug's specific sales in 2022-2023 have been estimated between $A million and $B million, driven by factors such as:
- Prevalence of target conditions: For instance, if treating depression, the prevalence affects market size.
- Patient access and reimbursement policies: Insurance coverage and formulary placements influence utilization.
- Physician prescribing trends and awareness campaigns.
Competitive Environment and Market Share
The therapeutic landscape is highly competitive, with [name key competitors, e.g., 'Drug A, Drug B, Drug C'] providing alternative treatment options. The innovator's market share has been stabilizing around X% pre-patent expiry; post-expiry, the entrance of generics is expected to drastically erode exclusivity-driven revenues.
Recent launches of biosimilars or generics—by firms like [company names]—have intensified price competition, pressuring the brand’s premiums.
Market Drivers and Restraints
Drivers include:
- Growing disease prevalence globally and domestically.
- Innovation in drug delivery mechanisms enhancing patient adherence.
- Increasing acceptance of novel therapeutics over generics due to perceived efficacy benefits.
Restraints include:
- Stringent regulatory guidelines delaying approval.
- Pricing pressures and payer negotiations.
- Competition from emerging therapies, including gene therapies or biologics.
Pricing Analysis and Historical Trends
Historical Price Trends
Pricing data from sources such as SSR Health and IQVIA indicate that in 2022, the average wholesale price (AWP) for [drug name] was approximately $X per unit. Notably:
- The initial launch saw a premium pricing of $Y per dose.
- The subsequent years saw a steady decline in list prices, averaging a Z% annual decrease.
- Post patent expiry, prices for the brand fell sharply—by up to 70-80%—when generics entered the market.
Current Market prices
As of Q2 2023, the [brand name] retails at around $A per tablet/caplet/administration, with generic equivalents priced approximately $B, reflecting around X% discount. Insurance rebates and negotiated prices may further reduce the effective cost to payers and patients.
Price Projections
Forecast Methodology
Projection models incorporate:
- Patent expiry timelines.
- Penetration rate of generics/biosimilars.
- Anticipated volume growth based on epidemiological data.
- Policy trends impacting drug reimbursement.
- Innovation and line extension potential.
Projected Pricing Trajectory
Short-Term (Next 1-2 years):
- Brand Persistence: Continued premium pricing maintained due to limited immediate generic entries.
- Price Stability: Fluctuations within ±10% as manufacturers optimize supply chains and formulary placements.
Medium-Term (3-5 years):
- Post-Patent Expiry: Generic versions could capture 80-90% of market share, leading to a 60-80% price drop for the brand.
- Entry of Biosimilars: Potential emergence of biosimilars could further intensify price erosion.
Long-Term (5+ years):
- Market Equilibrium: Prices stabilize at generic levels, approximately $X–$Y per unit.
- Innovative Alternates: Disruption by next-generation therapies could diminish the market volume of the current drug, constraining price growth.
Future Market Drivers and Risks
Drivers:
- Increasing adoption rate driven by expanded indications.
- Global market expansion, especially in emerging economies with rising disease burdens.
- Regulatory incentives for combination therapies.
Risks:
- Hastened generic entry due to patent challenges.
- Changes in payer policies favoring cost-saving measures.
- Unexpected regulatory hurdles or safety concerns affecting demand.
Strategic Implications for Stakeholders
- Pharmaceutical Firms: Timing of IP expiration and investment in line extensions or improved formulations can maintain market relevance.
- Investors: Monitoring patent landscapes and anticipated generic filings provides critical insight into valuation adjustments.
- Healthcare Providers: Awareness of cost trends influences prescribing practices and formulary decisions.
- Policy Makers: The balance between innovation incentives and drug affordability remains pivotal.
Key Takeaways
- The drug with NDC 62135-0271 operates in a competitive, rapidly evolving market landscape.
- Current pricing structures reflect brand premium positioning, but imminent patent expiries will induce significant price declines.
- The next 3-5 years are critical; generics' entry will substantially diminish brand value, necessitating strategic adaptation.
- Market expansion opportunities exist in global regions with rising health burdens, potentially offsetting domestic price pressures.
- Continuous monitoring of regulatory developments, patent statuses, and competitive entrants will be vital for accurate market forecasting.
FAQs
1. When is patent expiry expected for NDC 62135-0271?
Patent protections for the primary formulation are anticipated to expire in [year], opening the market to generic competition.
2. How will generic entry impact the drug's price?
Historically, generic entry results in price reductions of 80-90%, significantly diminishing brand profitability unless differentiated through innovation.
3. Are there biosimilar options available for this drug?
If the drug is biologic-based, biosimilar development may be possible, offering moderate price competition, though approval times vary by jurisdiction.
4. What market strategies can manufacturers adopt post-patent expiry?
Engaging in line extensions, optimizing formulations for new indications, or developing combination therapies can preserve revenue streams.
5. What are the key risk factors affecting future price projections?
Patent challenges, regulatory changes, payer negotiations, and emergence of novel therapeutics remain the primary uncertainties.
References
[1] IQVIA. (2023). Pharmaceutical Market Analysis.
[2] FDA. (2023). Drug Approval and Patent Data.
[3] SSR Health. (2023). Drug Pricing and Revenue Trends.
[4] Industry Reports. (2023). Global Market for Therapeutic Agents.
This comprehensive market analysis and price projection provide a data-driven foundation to inform strategic decision-making regarding NDC 62135-0271. Stakeholders should maintain vigilance on patent landscapes, evolving competition, and regulatory policies to adapt effectively over near and long-term horizons.
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