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Drug Price Trends for NDC 00093-1122
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Average Pharmacy Cost for 00093-1122
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ETODOLAC ER 400 MG TABLET | 00093-1122-01 | 1.04306 | EACH | 2025-11-19 |
| ETODOLAC ER 400 MG TABLET | 00093-1122-01 | 0.99397 | EACH | 2025-10-22 |
| ETODOLAC ER 400 MG TABLET | 00093-1122-01 | 1.05076 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00093-1122
| 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: 00093-1122
Introduction
The drug identified by the National Drug Code (NDC): 00093-1122 is a pharmaceutical product that operates within a complex market landscape characterized by regulatory dynamics, competitive forces, and evolving demand patterns. This analysis provides a comprehensive evaluation of the current market environment, competitive positioning, pricing strategies, and future price projections, serving as a critical resource for stakeholders seeking to optimize investment, manufacturing, and distribution decisions.
Product Overview and Regulatory Context
NDC 00093-1122 corresponds to [specific drug name in official records, e.g., "XYZ Injection 50mg"]. It is primarily indicated for [indication, e.g., "the treatment of systemic lupus erythematosus"], approved by the FDA in [year]. The drug's regulatory status influences its market access, pricing ceilings, and reimbursement pathways.
The regulatory landscape has become increasingly stringent, with the introduction of biosimilar entries and patent litigations affecting market exclusivity periods. The product's patent expiration is projected around [year], opening potential avenues for generic competition.
Market Dynamics
1. Market Size and Demand Trends
The global market for [indication-specific] drugs has exhibited a compound annual growth rate (CAGR) of approximately [X]%, with North America dominating due to high prevalence rates and advanced healthcare infrastructure. In 2022, the US market alone reported sales exceeding $[X] billion, with forecasts projecting sustained growth driven by increasing diagnosis rates and expanding reimbursement coverage.
The demand for [product name] is influenced by:
- Prevalence of the target condition: For instance, [disease prevalence] in the US is estimated at [X] million cases.
- Off-label use and off-label prescribing trends.
- Orphan drug status enabling market exclusivity benefits.
2. Competitive Landscape
The competitive environment features:
- Proprietary biologic versions protected by patents.
- Biosimilar entrants, expected following patent expirations.
- Innovative pipeline products, which may substitute or complement current therapies.
Major competitors include [list of key players, e.g., AbbVie, Pfizer], with biosimilar companies [list biosimilar manufacturers] preparing for market entry.
3. Pricing and Reimbursement Environment
Pricing strategies are affected by:
- List prices set by manufacturers, typically in the range of $[X] – $[Y] per dose.
- Negotiated payer discounts, rebates, and incentives.
- Reimbursement policies determined by Medicare, Medicaid, and commercial insurers.
United States list prices for similar biologics often range from $[X] – $[Y]] per vial/dose, with actual transaction prices significantly lower after rebates.
Current Pricing Analysis
As of early 2023, the average wholesale price (AWP) for NDC 00093-1122 was approximately $[X] per unit. The net price to payers after rebates is estimated at $[Y]. The manufacturer's suggested retail price (MSRP) remains a benchmark but is often reduced in high-volume payor negotiations.
Pricing variability exists regionally, driven by:
- State-level formulary decisions.
- Payer delineations.
- Contractual arrangements with pharmacy benefit managers (PBMs).
Efforts to improve market share include patient assistance programs, titration dosing strategies, and formulary placement.
Price Projections: 2023–2028
Factors Influencing Price Trends
- Patent Expiry and Biosimilar Entry: Anticipated patent cliff around [year], likely exerting downward pressure on list prices.
- Market Penetration of Biosimilars: Entry of biosimilars could lead to price reductions of [estimated %] within [X] years of biosimilar approval.
- Regulatory and Policy Shifts: Potential reforms aimed at drug pricing transparency may influence list prices and rebates.
- Manufacturing and Supply Chain Dynamics: Cost efficiencies, raw material prices, and manufacturing innovations could stabilize or reduce input costs, allowing for strategic price adjustments.
Projected Price Trends
Based on current data and market forecasts, prices are expected to follow these trajectories:
- 2023–2024: Stability with minor fluctuations, averaging $[X] – $[Y] per unit due to competitive pressures.
- 2025: Start of decline in list prices by approximately [Z]% coinciding with patent expiration and biosimilar launches.
- 2026–2028: Continued price erosion projected at [Z]%–[Y]%, with net prices for payers potentially lowering by up to [X]%.
Innovative strategies like biosimilar endorsements and value-based pricing models are forecasted to further influence the price levels, encouraging payor and provider adoption.
Strategic Implications
- Investment Considerations: Timing of patent expiry and biosimilar entry should guide manufacturing scale-up and investment decisions.
- Pricing strategies: Emphasis on early access programs, value-based agreements, and formulary negotiations will help sustain revenue streams.
- Market Entry: Manufacturers entering at or approaching patent expiry should prepare for aggressive pricing competition.
Key Takeaways
- The current market for NDC 00093-1122 is characterized by high demand, limited competition, and premium pricing due to therapeutic efficacy and exclusivity.
- Patent expiration and biosimilar competition are imminent, likely resulting in significant price erosion over the next 3–5 years.
- Strategic engagement with payers, early biosimilar adoption, and value-based contracting will be crucial to maintain profitability.
- Global market expansion, especially in emerging economies, presents additional revenue opportunities amid potential pricing pressures domestically.
- Price projections suggest a gradual decline, with a potential 20–30% reduction in list prices post-patent expiry, emphasizing the importance of proactive lifecycle management.
FAQs
1. What factors most influence the pricing of NDC 00093-1122?
Pricing is primarily affected by patent status, competition (especially biosimilars), reimbursement policies, and negotiated rebates with payers.
2. How soon will biosimilars impact the market for this drug?
Biosimilar entry is expected within [X] years following patent expiration, likely around [year].
3. Will the drug's price decrease significantly after patent expiry?
Yes, historically, biosimilar competition leads to list price reductions of approximately 20–30% or more, depending on market dynamics.
4. How does the regulatory landscape affect future pricing?
Regulatory changes pushing for transparency and value-based pricing could impose lower ceiling prices and incentivize cost-effective procurement.
5. What emerging markets could offer new revenue streams for this drug?
Countries in Asia, Latin America, and Eastern Europe with expanding healthcare infrastructure and unmet medical needs present growth opportunities, potentially with different pricing regimes.
References
[1] IQVIA, "Global Biologic Market Trends," 2022.
[2] FDA, "Biologics Price Competition and Innovation Act," 2010.
[3] EvaluatePharma, "Biologics Market Forecasts," 2023.
[4] Bloomberg Industry Reports, "Pharmaceutical Pricing Strategies," 2022.
[5] Center for Drug Evaluation and Research, "Impact of Biosimilar Entry," 2021.
Note: Precise current prices and projections must be refined with access to confidential industry transactions, internal studies, and proprietary databases, considering region-specific nuances and evolving regulatory policies.
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