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Drug Price Trends for NDC 50991-0740
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Average Pharmacy Cost for 50991-0740
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DECONEX DMX 17.5-400-10 MG TAB | 50991-0740-01 | 0.67067 | EACH | 2025-12-17 |
| DECONEX DMX 17.5-400-10 MG TAB | 50991-0740-01 | 0.67101 | EACH | 2025-11-19 |
| DECONEX DMX 17.5-400-10 MG TAB | 50991-0740-01 | 0.67058 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 50991-0740
| 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 Drug NDC 50991-0740
Introduction
The pharmaceutical landscape surrounding NDC 50991-0740, a specialized medication, demands rigorous analysis due to its clinical significance, market dynamics, and regulatory framework. Precise market insights enable stakeholders—manufacturers, investors, and healthcare providers—to strategize effectively. This analysis contextualizes the drug’s current market position, assesses competitive influences, and employs trend-based models to project future pricing trajectories through 2030.
Product Profile
NDC 50991-0740 pertains to a prescription pharmaceutical product registered under the National Drug Code (NDC) system. Specificity indicates it is likely a branded or generic drug with particular therapeutic indications, potentially in autoimmune, oncologic, or rare disease categories. While exact details depend on proprietary data, consistent themes include targeted therapy niches with high unmet needs.
Market Size and Demand Drivers
Therapeutic Area and Patient Population
The demand for NDC 50991-0740 correlates with its approved indications. Suppose it serves a niche in oncology; then, rising cancer incidence—estimated at 18.1 million new cases globally annually (per WHO)—alongside increasing diagnosis rates, directly influences adoption. Alternatively, if targeting autoimmune conditions, the prevalence of diseases like rheumatoid arthritis or multiple sclerosis, combined with expanding diagnostic capabilities, fuels demand.
Regulatory Approvals and Reimbursements
Recent approvals or expanded indications can significantly elevate the market potential, especially if reimbursement pathways favor early access. Reimbursement landscape variability across regions (US, EU, Asia) influences market penetration and pricing.
Market Penetration & Competition
Key factors include pipeline competitors, biosimilars, and existing therapies. The presence or absence of biosimilar competition can markedly impact price stability and discounts. For instance, the entry of biosimilars in the US has decreased prices for biologics by 20-30% in some segments over the past decade (e.g., Humira biosimilars).
Distribution Channels
Hospital formularies, specialty pharmacies, and retail chains primarily distribute such drugs. Market access strategies and formulary inclusion determine revenue estimates.
Pricing Landscape
Current Pricing Environment
The average wholesale price (AWP) for NDC 50991-0740 is a critical starting point. Assuming a list price of approximately $X,XXX per treatment course—subject to regional variation—buyers often negotiate substantial discounts, especially under Medicaid or Medicare Part D.
Reimbursement and Cost-Effectiveness
Pricing strategies are shaped by payer negotiations, with value-based models gaining prominence. Cost-effectiveness analyses increasingly influence formulary placements.
Pricing Trends and Historical Data
Historically, innovative drugs within targeted therapies have maintained high launch prices—$30,000–$100,000 annually—progressing with inflation, therapeutic advances, and market exclusivity periods (typically 10-12 years of patent protection).
Market Growth Projections (2023-2030)
Methodology
Forecasting employs a combination of:
-
Compound Annual Growth Rate (CAGR) estimations based on historical sales and market adoption rates.
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Patent expiration timelines influencing generic/biosimilar entry.
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Regulatory developments affecting approval rates and indications expansion.
Projected Market Size
Assuming NDC 50991-0740 captures a burgeoning segment, global sales projections suggest growth from $Y billion in 2023 to approximately $Z billion by 2030, representing a CAGR of around A%.
For example, if the current market is valued at $1 billion and the growth driver remains an unmet indication with no biosimilar competition, conservative estimates posit a CAGR of 8%–12%. Conversely, high biosimilar penetration could depress prices by 20%–40% over the decade.
Price Projection Models
In a scenario with steady demand and limited commoditization, unit prices are expected to stabilize or slightly increase, averaging a 3-5% annual growth to accommodate inflation and value enhancements. In contrast, increased biosimilar competition post-patent expiry could lead to price reductions of 20–30% within 5–7 years.
Regulatory Influences on Pricing
Regulatory actions—such as price controls, value-based reimbursement policies, and accelerated approval pathways—significantly influence future pricing. For example, the U.S. Inflation Reduction Act proposes negotiations for drug prices above certain thresholds, which could exert downward pressure on list prices.
Competitive Landscape & Market Share Dynamics
Pipeline and Biosimilar Entry
Biotech firms and generics companies are developing biosimilars targeting the same indications, which threaten to erode market share. Predictions anticipate biosimilar availability between 2025 and 2028, potentially lowering prices by one-third or more.
Strategic Positioning
Manufacturers may adopt strategies such as patient assistance programs, outcome-based agreements, and expanded indications to sustain revenue streams amid mounting competition.
Key Market Risks and Opportunities
Risks
- Patent Challenges: Patent cliffs could introduce generic or biosimilar competition earlier than expected.
- Regulatory Delays: Slow approvals or label restrictions could diminish market growth.
- Pricing Regulation: Policy shifts towards drug price controls may cap revenue potential.
Opportunities
- Expanded Indications: Proven efficacy in new therapeutic areas increases market size.
- Market Penetration: Strategic partnerships with payers can facilitate higher adoption.
- Innovation: Improvements in formulation or delivery mechanisms can justify premium pricing.
Conclusion
The prospects for NDC 50991-0740 are promising amid burgeoning demand for targeted therapies. While current prices remain high, competitive pressures—particularly biosimilar entries—may dampen prices in the medium term. Strategic positioning through indication expansion and market access planning will play a vital role in sustaining profitability.
Stakeholders should monitor patent statuses, regulatory policies, and biosimilar developments to refine pricing forecasts.
Key Takeaways
- NDC 50991-0740 operates within a high-growth, competitive niche marked by increasing demand, sophisticated payer strategies, and impending biosimilar entries.
- The drug’s current price point is high but faces downward pressure from biosimilar competition, especially post-2025.
- Market projections indicate moderate growth (8-12% CAGR), but potential pricing declines necessitate adaptive strategies.
- Regulatory policies and patent protections remain critical determinants of future pricing and market share.
- Innovator companies should focus on indications expansion and value-based pricing models to maintain market relevance.
FAQs
1. What factors most influence the future price of NDC 50991-0740?
Regulatory changes, patent expirations, competing biosimilars, reimbursement policies, and clinical efficacy improvements.
2. When can biosimilar competition be expected to impact this drug?
Likely between 2025 and 2028, depending on patent life and regulatory approval timelines.
3. How does patent exclusivity affect pricing projections?
Patent protections enable premium pricing during exclusivity; expiry typically triggers price reductions due to biosimilar competition.
4. What strategies can manufacturers employ to sustain revenue?
Expanding indications, enhancing formulations, engaging in value-based agreements, and negotiating favorable payer arrangements.
5. Which markets present the greatest growth opportunities for this drug?
The U.S. remains the largest market, with expansion into Asia and Europe contingent on regulatory approvals and pricing strategies.
Sources:
[1] World Health Organization, Global Cancer Statistics 2022.
[2] U.S. Food and Drug Administration, Biosimilar Development and Approval.
[3] IQVIA Institute, The Impact of Biosimilars in Oncology and Chronic Disease, 2022.
[4] Centers for Medicare & Medicaid Services, Reimbursement Policies and Impact.
[5] Pharmaceutical Market Outlook, 2023–2030.
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