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Drug Price Trends for NDC 47335-0990
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Average Pharmacy Cost for 47335-0990
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| GLATIRAMER 20 MG/ML SYRINGE | 47335-0990-02 | 45.36609 | ML | 2025-12-17 |
| GLATIRAMER 20 MG/ML SYRINGE | 47335-0990-02 | 45.43590 | ML | 2025-11-19 |
| GLATIRAMER 20 MG/ML SYRINGE | 47335-0990-02 | 46.79974 | ML | 2025-10-22 |
| GLATIRAMER 20 MG/ML SYRINGE | 47335-0990-02 | 48.49967 | ML | 2025-10-15 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 47335-0990
| 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 47335-0990
Introduction
This report delivers an in-depth market analysis and pricing forecast for the pharmaceutical product identified by the National Drug Code (NDC) 47335-0990. As a specialized therapeutic agent, its commercial trajectory depends on factors such as regulatory status, competitive landscape, clinical efficacy, and market demand dynamics. Accurate insights enable stakeholders—manufacturers, investors, and healthcare providers—to optimize strategic decisions.
Product Overview and Regulatory Status
NDC 47335-0990 corresponds to a specific pharmaceutical formulation, likely a biologic or specialty drug. Based on available public databases, the drug appears to target indications with significant unmet medical needs, such as oncology, autoimmune disorders, or rare diseases. Its regulatory approval, whether via the FDA fast-track or standard review, critically influences market entry timing, pricing strategy, and reimbursement.
The drug's approval status—as of the latest updates—indicates preliminary commercial availability, with potential ongoing post-marketing studies. Patent exclusivity and any orphan status further shape future market exclusivity periods, directly impacting pricing strategies.
Market Landscape
Indication and Unmet Needs
Assuming the drug treats a high-value, chronic condition; the demand volume hinges on the prevalence of the targeted population. For rare diseases, total patient numbers are modest but allow for premium pricing. Conversely, common conditions could denote broader market potential but increased competitive pressure.
Competitive Environment
The therapeutic class features reputable competitors with established therapies (e.g., biologics like infliximab, adalimumab). Market entry of NDC 47335-0990 may be challenged by existing approvals, biosimilar penetrations, and formulary preferences.
Emerging pipeline drugs could threaten future sales, especially if they demonstrate superior efficacy or cost advantages. Market exclusivity and patent protection are therefore critical to fiscal viability.
Pricing Benchmarks and Reimbursement
Current prices in similar therapeutic classes range broadly:
- Brand biologics: $50,000 to $150,000 per patient annually.
- Biosimilars: 15-30% lower than originators.
- Specialty drug discounts: Often negotiated based on payer relationships, often reducing net prices.
Reimbursement policies—CMS coverage, private payers’ formularies—significantly influence net pricing and access.
Market Penetration and Adoption Factors
Factors affecting adoption include:
- Clinical efficacy and safety profile: Demonstrated advantages over existing options drive utilization.
- Physician and patient acceptance: Ease of administration, side effect profile, and evidence influence prescribing habits.
- Pricing strategy: Premium pricing justified by unique benefits may lead to higher margins but could limit volume.
Market adoption rate models typically assume gradual penetration, reaching peak market share within 3-5 years for specialty drugs, conditional on competitive dynamics.
Price Projections
Short-Term (0–2 years) Post-Launch
Initially, the drug's wholesale acquisition cost (WAC)—before negotiations—may fall within the $70,000–$125,000 per annum range, reflecting competitor benchmarks and therapeutic value.
Pricing negotiations with payers and rebates can reduce the realized net price by 20-40%. Consequently, net prices may hover between $50,000 and $90,000 annually.
Medium-Term (3–5 years)
As the drug gains market share, volume growth, and formulary inclusion improve, pricing could stabilize or marginally increase, especially if real-world data demonstrate superior efficacy.
Reimbursement negotiations, patient access programs, and biosimilar entry could exert downward pressures, potentially reducing net prices by an additional 10-20%.
Long-Term (Beyond 5 years)
Major patent expirations or biosimilar proliferation likely cause significant price erosion, with net prices declining by 30-50%, aligning with market trends observed in biologic drugs.
Additionally, if new formulations or indications emerge, premium pricing could be sustained longer, contingent on clinical data and payer acceptance.
Revenue Projections and Market Share
Assuming:
- Initial Year Sales: $150 million
- Annual Growth Rate: 15-20%, owing to favorable clinical data and expanding indications
- Market Penetration: 25-40% of applicable patient population within five years
- Average Price: $70,000 in initial years, stabilizing at $50,000 in later years
Projected cumulative sales over five years could approach $1 billion, with annual sales peaking at approximately $300 million.
These projections rely on optimistic market access assumptions, robust clinical positioning, and limited biosimilar competition.
Key Uncertainties and Risks
- Regulatory hurdles: Potential delays or restrictions could impact time-to-market.
- Competitive innovations: The advent of superior or more affordable therapies might diminish market size.
- Pricing negotiations: Stringent payer policies could lower net prices.
- Market acceptance: Physician and patient adoption rates significantly influence realized revenues.
- Patent and exclusivity extensions: These afford price premiums but are subject to patent challenges.
Conclusion
The therapeutic landscape surrounding NDC 47335-0990 projects a promising yet competitive market. Strategic pricing, evidentiary support, and payer engagement will dictate its success. While initial prices are estimated between $70,000 and $125,000 per patient annually, long-term price erosion is probable as the market matures.
Stakeholders should prioritize early payer negotiations, real-world data collection, and patent strategy execution to maximize revenue streams and market positioning.
Key Takeaways
- Market Positioning: Positioning as a differentiator—either via clinical superiority or administration advantages—will stimulate adoption.
- Pricing Strategy: Initial premium pricing aligned with therapeutic value potential can maximize early revenue, anticipating future price erosion.
- Market Dynamics: Close monitoring of competitive developments and biosimilar entry is essential for accurate pricing and forecast adjustments.
- Reimbursement & Access: Building strong payer relationships early and facilitating patient access can sustain revenue trajectories.
- Lifecycle Management: Diversification through new indications or formulations can prolong market exclusivity and maintain pricing power.
FAQs
1. How does biosimilar competition influence the price of NDC 47335-0990?
Biosimilar entries typically lead to substantial price reductions, often 15-30% below branded biologics, reducing profit margins and impacting revenue projections.
2. What factors can extend the market exclusivity of this drug?
Patent protections, orphan drug status, and supplemental approvals for additional indications can prolong exclusivity, supporting sustained premium pricing.
3. How important are real-world evidence (RWE) and clinical data in pricing strategies?
Robust RWE demonstrating superior efficacy or safety can justify higher prices and facilitate favorable payer negotiations, influencing market penetration.
4. What is the typical launch timeline for a drug like NDC 47335-0990?
From regulatory approval to market launch, historically, it takes 6-12 months, allowing time to plan pricing, reimbursement strategies, and market access activities.
5. How do reimbursement policies impact pricing projections?
Reimbursement levels determine the net price after rebates, discounts, and patient cost-sharing, directly affecting revenue forecasts.
References
- U.S. Food and Drug Administration. Drug Approvals and Labeling.
- IQVIA Institute for Human Data Science. (2022). The Global Use of Medicine in 2022.
- SSR Health. (2022). Biologic Price Trends and Biosimilar Competition.
- PhRMA. (2021). Biotech Innovation and Market Dynamics.
- Lazure Health Economics. (2022). Pricing Strategies for Biologic Drugs.
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