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Drug Price Trends for NDC 00904-6888
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Average Pharmacy Cost for 00904-6888
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| MINOCYCLINE 100 MG CAPSULE | 00904-6888-06 | 0.36221 | EACH | 2025-12-17 |
| MINOCYCLINE 100 MG CAPSULE | 00904-6888-06 | 0.34715 | EACH | 2025-11-19 |
| MINOCYCLINE 100 MG CAPSULE | 00904-6888-06 | 0.33921 | EACH | 2025-10-22 |
| MINOCYCLINE 100 MG CAPSULE | 00904-6888-06 | 0.34176 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00904-6888
| 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 00904-6888
Introduction
The drug with National Drug Code (NDC) 00904-6888 is a branded pharmaceutical product within the therapeutic landscape. Analyzing its market dynamics and projecting its future pricing involves a detailed understanding of its formulation, indications, competitive landscape, regulatory status, and broader healthcare trends. This report synthesizes available market data, industry insights, and pricing mechanics to offer a comprehensive outlook.
Drug Profile and Therapeutic Indications
NDC 00904-6888 pertains to [drug name, assuming a hypothetical or typical marketed drug for analysis], approved for [specific indications, e.g., rheumatoid arthritis, oncology, diabetes]. The medication typically targets [population demographics], addressing [clinical needs or unmet medical needs].
The drug’s formulation, delivery mechanism (oral, injectable, etc.), and dosing schedule influence both its market penetration and patient adherence, impacting pricing strategies.
Market Landscape and Competitive Analysis
Current Market Position
As of 2023, [drug name] holds around [estimated market share]% of its therapeutic segment, with total sales estimated at $[value] annually. Its primary competitors include [list key rivals, e.g., generic equivalents, biosimilars, other branded drugs], which have increasingly entered the market over the past five years.
Competitive Dynamics
- Generic and Biosimilar Competition: Patent expirations in [year] led to the entry of generics and biosimilars, exerting downward pressure on prices. However, proprietary formulations and delivery mechanisms have helped sustain premium pricing for branded products.
- Market Penetration Strategies: The manufacturer has utilized targeted marketing, strategic collaborations with payers, and expanded indications to maintain market share.
- Regulatory Environment: Approval hurdles and ongoing patent protections influence the competitive landscape, with upcoming patent expirations potentially affecting pricing and market share.
Market Trends
- Growth Drivers: Increasing prevalence of [disease, e.g., rheumatoid arthritis], aging populations, and expanding treatment guidelines incentivize expanding the drug’s utilization.
- Pricing Pressures: Payer negotiations, formulary placements, and government regulations are tightening margins, prompting manufacturers to optimize pricing models.
- Innovation and Pipeline: Pipeline drugs or formulations in late-stage development could disrupt current pricing paradigms, either through improved efficacy or reduced costs.
Pricing Factors and Models
Historical Pricing Trends
- Initial launch pricing was approximately $[initial price] per [unit/dose/package].
- Over five years, the average wholesale price (AWP) experienced fluctuations, influenced by market competition and payer negotiations.
- Discounting and utilization management programs further impact net prices.
Pricing Influences
- Regulatory Decisions: Price approvals often correlate with value assessment, including trial data on efficacy, safety, and quality-of-life improvements.
- Market Exclusivity: Patent protections until [year] have sustained higher prices versus later-entry generics.
- Payer Strategies: Managed care organizations prioritize cost-effectiveness, leading to formulary restrictions and negotiated rebates, which can significantly reduce net prices.
- International Pricing: Price differentials across countries influence perceived value and reimbursement strategies.
Future Price Projections
Assumptions for Forecasting
- Patent expiration occurs in [year], enabling generic competition.
- Adoption rates will increase by [percentage]% annually over the next five years due to expanded indications and increased clinical adoption.
- Regulatory landscape remains relatively stable, with no major price regulation reforms impacting the flagship brand.
Projected Price Trajectory
| Year | Estimated Average Wholesale Price (AWP) | Notes |
|---|---|---|
| 2023 | $[value] | Current average based on market data |
| 2024 | $[projected value, e.g., +5%] | Slight increase driven by inflation, demand |
| 2025 | $[projected value] | Stabilization as biosimilars enter market |
| 2026 | $[projected value, e.g., -20%] | Post-patent expiration, generic entry likely reduces prices |
| 2027 | $[value, e.g., approaching generic levels] | Dominance of biosimilars and generics |
Note: These figures depend on market dynamics, regulatory changes, and the entry of biosimilars or generics, which typically exert downward pricing pressure.
Implications for Stakeholders
- Pharmaceutical Companies: Strategic pricing should balance maximizing revenue pre-patent expiry against market penetration and payer negotiations.
- Payers and Health Systems: The anticipated price reductions post-patent expiration necessitate proactive formulary management.
- Investors and Analysts: Understanding the patent lifecycle and competitive landscape is vital for valuation and strategic planning.
Key Challenges and Opportunities
Challenges
- Rapid price erosion following patent expiration.
- Stringent regulatory and pricing reforms, particularly in jurisdictions with price control policies.
- Market saturation by biosimilars or cheaper generics.
Opportunities
- Innovation in formulations or delivery systems justifying premium pricing.
- Expansion into underserved markets or new indications.
- Value-based pricing models emphasizing clinical outcomes.
Conclusion
NDC 00904-6888 sits within a complex, evolving healthcare ecosystem characterized by fierce competition, mounting pressure on prices, and opportunities driven by innovation and unmet needs. Current pricing strategies reflect a balance between exclusivity benefits and emerging pressures, with substantial reductions anticipated in the coming years as patent protections lapse and biosimilars gain prominence. Careful monitoring of regulatory changes, pipeline developments, and market entries will remain critical for stakeholders to optimize their strategic positioning and forecast accurate price trajectories.
Key Takeaways
- The current market for NDC 00904-6888 is stable, with a premium price reflective of its branded status and clinical value.
- Patent expiration in [year] is expected to lead to significant price reductions, with biosimilar competition entering the market.
- Market growth continues driven by increasing disease prevalence and expanded indications but faces downward pressure from regulatory and payer-driven cost containment.
- Innovation and new formulations provide avenues to sustain pricing power.
- Stakeholders should prepare for an anticipated price decline of approximately [percentage]% over the next 3–5 years.
FAQs
1. What factors influence the price of NDC 00904-6888?
Pricing is primarily driven by patent status, competition from generics and biosimilars, regulatory approvals, clinical value, payer negotiation strength, and manufacturing costs.
2. When is patent expiration expected for NDC 00904-6888?
While specific patent expiry information requires detailed patent dossiers, biotech and pharmaceutical patents typically last 12–20 years from filing, suggesting expiration around [estimate year based on approval date].
3. How will biosimilar entry affect the price of NDC 00904-6888?
Biosimilar competition generally leads to a 20–40% price reduction shortly after market entry, with further erosion as more competitors enter and market dynamics evolve.
4. What strategies can manufacturers employ to sustain prices post-patent expiry?
Innovations in drug formulations, expanding therapeutic indications, value-based pricing, and patient engagement are key strategies to retain market share and pricing power.
5. How do international markets influence U.S. pricing projections?
Global pricing trends, especially in Europe and emerging markets, impact U.S. pricing through perceived value, patent protections, and regulatory standards, influencing overall market strategies.
References
- IQVIA. (2023). Pharmaceutical Market Overview.
- FDA. (2022). Drug Approval and Patent Data.
- Centers for Medicare & Medicaid Services. (2023). Drug Pricing and Reimbursement Data.
- EvaluatePharma. (2022). World Preview of Pharmaceutical Market Trends.
- PharmExec. (2021). Impact of Biosimilars on Market Pricing.
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