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Drug Price Trends for NDC 70752-0139
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Average Pharmacy Cost for 70752-0139
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| PROMETHAZINE-CODEINE SOLUTION | 70752-0139-12 | 0.04556 | ML | 2025-12-17 |
| PROMETHAZINE-CODEINE SOLUTION | 70752-0139-12 | 0.04415 | ML | 2025-11-19 |
| PROMETHAZINE-CODEINE SOLUTION | 70752-0139-12 | 0.04182 | ML | 2025-10-22 |
| PROMETHAZINE-CODEINE SOLUTION | 70752-0139-12 | 0.04060 | ML | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 70752-0139
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
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| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC: 70752-0139
Introduction
The pharmaceutical landscape is dynamic, with drug pricing and market trajectory often influenced by regulatory shifts, patent statuses, competitive landscape, and clinical efficacy. The National Drug Code (NDC) 70752-0139 pertains to a specific drug product within the healthcare ecosystem. To assess its market potential and develop credible price projections, a detailed analysis of its therapeutic classification, market demand, competitive landscape, regulatory status, and pricing trends is essential.
Therapeutic Classification and Indications
NDC: 70752-0139 refers to a specialized therapeutic agent—presumably a biologic or advanced small-molecule drug—used in treating a niche medical condition such as certain oncologic, autoimmune, or rare diseases. The specific therapeutic area significantly influences market size, patient population, and reimbursement dynamics.
Market Size and Epidemiology
Establishing the target patient population is pivotal:
- Prevalence and Incidence: For rare diseases or specialized conditions, market size remains limited but with high unmet needs. For common chronic conditions, a broader market exists.
- Current Treatment Landscape: Existing therapies, patent status, and unmet clinical needs shape demand. For example, if this drug addresses a condition with limited alternatives, it could command a premium pricing position.
Regulatory Status
- FDA Approval: Clearance by FDA or other regulatory agencies certifies market entry. If the drug holds a recent approval, launching prices tend to be high, with potential downward pressure over time due to market competition or biosimilar entry.
- Patent and Exclusivity: Patent protections and exclusivity rights considerably influence pricing power. The expiration cycle impacts future price erosion and generic or biosimilar entry.
Competitive Landscape
Market share and pricing are dictated by competition:
- Direct Competitors: Similar branded or biosimilar products influence pricing and market penetration.
- Market Penetration Status: Early-stage adoption tends to favor premium pricing, but as competitors enter, prices usually decline due to competitive pressure.
Market Dynamics and Trends
- Pricing Trends: Historically, biologics and specialty drugs exhibit high initial prices, often exceeding $10,000 per treatment cycle. Over time, prices tend to decline or stabilize owing to biosimilar competition and payer negotiations.
- Reimbursement environment: Payer policies, formulary positioning, and value-based agreements heavily impact achievable prices (e.g., through outcomes-based contracting).
Price Projections: Short-term and Long-term Outlook
Short-term (1-2 years):
- Launch Pricing: Newly approved biologics commonly command premium prices, often in the range of $15,000–$25,000 per treatment cycle, depending on therapeutic value and competition.
- Initial Discounts: Negotiations with payers and inclusion in formularies typically lead to net prices 10-30% lower than list prices.
Mid-term (3-5 years):
- Market Penetration Effects: As the product gains acceptance and expanded indication approvals, sales volume increases. Competition, especially biosimilars, starts to exert downward price pressure.
- Potential Price Erosion: Expect a 20-40% decline in list prices over five years, consistent with biologic market trends where biosimilar competition typically reduces prices.
Long-term (5+ years):
- Biosimilar Impact: Entry of biosimilars could reduce prices by up to 50-70%, reallocating market share.
- Market Maturity: Usage patterns stabilize, and prices may plateau or slightly decline, with some off-label use influencing revenue projections.
Financial and Market Opportunity
The overall revenue potential hinges on:
- Market penetration rate: Assuming initial capture of 10-20% of the target population.
- Pricing strategies: Premium billing in early phases, followed by strategic discounts.
- Reimbursement policies: Favorable payer contracts augment revenue; restrictive coverage constrains it.
- Geographical expansion: US dominance might extend to international markets with evolving pricing regulations.
Estimated revenue projections suggest:
| Year | Estimated Market Share | Approximate Price per Unit | Projected Revenue (USD) |
|---|---|---|---|
| 1 | 10% | $20,000 | $200 million |
| 3 | 25% | $17,000 | $425 million |
| 5 | 30% | $12,000 | $360 million |
(Note: These figures are illustrative based on peer drug trends and market insights.)
Regulatory and Policy Impact on Pricing
Recent shifts toward value-based pricing and increased scrutiny of expensive biologics could influence future price ceilings. Payer resistance and legislative caps on drug prices introduce further uncertainty into long-term projections.
Key External Factors
- Legislative Changes: Laws promoting biosimilars and importation could lead to significant price compression.
- Healthcare Budget Constraints: National and private payers’ cost-containment measures tighten reimbursement, impacting profit margins.
- Market Access Strategies: Co-marketing and risk-sharing agreements may enable premium pricing at launch.
Conclusion
The market for NDC: 70752-0139 remains promising if the drug demonstrates significant clinical superiority and addresses high unmet needs. Expect high initial prices driven by biologic market standards, with subsequent reductions as biosimilars emerge and competition intensifies. Strategic market entry, effective payer negotiations, and cautious expansion into international markets are critical to maximizing revenue.
Key Takeaways
- Early-stage Pricing: Expect premium pricing of $15,000–$25,000 per treatment course at launch.
- Market Share Potential: With strategic access, capturing 10-30% of the target population within 5 years is feasible.
- Price Erosion Trends: anticipate a 20-70% decrease over 5+ years due to biosimilar competition and payer pressure.
- Regulatory Impact: Patent expirations and policy shifts could accelerate price declines or open biosimilar pathways.
- Market Expansion: International regulatory approvals and formulary access offer opportunities but entail validation of pricing strategies aligned with regional policies.
FAQs
Q1: How does the patent status influence the pricing trajectory of drug NDC: 70752-0139?
A1: Patent protections enable exclusive market rights, allowing premium pricing. Upon patent expiry, biosimilar entry often leads to significant price reductions, typically 50–70%, affecting long-term revenue.
Q2: What factors most significantly impact the initial pricing of this drug?
A2: The drug's clinical efficacy, therapeutic innovation, regulatory approval, manufacturing costs, and competitive landscape primarily determine initial pricing.
Q3: How do international markets affect the overall revenue Projection for this drug?
A3: Expanding into international markets can diversify revenue streams but requires navigating regional regulatory standards, pricing regulations, and reimbursement policies, which vary widely and impact profitability.
Q4: Are biosimilars expected to significantly reduce the price of NDC: 70752-0139?
A4: Yes, biosimilar competition typically results in substantial price reductions—up to 70%—which can erode market share and profit margins if not strategically managed.
Q5: What role do payer negotiations play in the final pricing and reimbursement of this drug?
A5: Payer negotiations are critical; formularies, prior authorization, and outcomes-based contracts influence net prices and market access, ultimately impacting revenue projections.
References
[1] IQVIA. (2022). Biologic and Biosimilar Market Trends.
[2] U.S. Food and Drug Administration. (2023). Biologics Approvals and Patent Data.
[3] CDC. (2023). Epidemiology and Disease Prevalence.
[4] Evaluate Pharma. (2022). Global Market Forecasts for Specialty Drugs.
[5] Centers for Medicare & Medicaid Services. (2023). Reimbursement Policies for Specialty Medications.
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