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Last Updated: April 16, 2026

Drug Price Trends for NDC 46122-0423


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Best Wholesale Price for NDC 46122-0423

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Dates Price Type
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Market Analysis and Price Projections for NDC 46122-0423

Last updated: April 3, 2026

What is NDC 46122-0423?

NDC 46122-0423 is a marketed drug identified by the National Drug Code (NDC). It is a prescription medication approved for specific indications (exact drug name, formulation, and use are needed for a complete profile). This code designates a single product, its manufacturer, and packaging details. Precise market data and price projections depend on the drug's therapeutic class, market competition, and patent status.

Market Landscape

Therapeutic Category and Indications

  • The drug's therapeutic class influences market size and competition.
  • Approved indications impact prescribing volume and patient base.
  • Recent approvals or label expansions can shift market dynamics.

Market Size and Growth

  • Estimated market size based on current prescriptions, patient populations, and disease prevalence.
  • Growth rate projections depend on factors such as:

    • Incidence and prevalence of the target condition.
    • Competitive landscape including generics and biosimilars.
    • Adoption rates driven by efficacy, safety, and reimbursement.

Competitive Environment

Company Drug Name Formulation Market Share Patent Status
Company A Drug X 50 mg tablets 55% Patent valid until 2030
Company B Drug Y 100 mg capsules 40% Patent expired 2022
Biotech Z Biosimilar W Injection 5% Pending biosimilar approval

Regulatory and Reimbursement Factors

  • Health authority approvals (FDA, EMA, etc.) impact market access.
  • Reimbursement policies, coverage restrictions, and formulary placements influence sales.

Price Projections

Current Pricing Data

  • Brand drug average wholesale price (AWP): $X per unit (e.g., tablet, vial).
  • Typical dosing regime: Y units per day.
  • Estimated annual treatment cost for the average patient: $Z.

Factors Influencing Future Prices

  • Patent expiration and generic entry typically reduce prices by 30-80%.
  • Biosimilar or competing formulations can further decrease costs.
  • Market demand growth can support stable or slightly increasing list prices.

Projected Price Trends

Year Estimated Average Price Key Drivers
2023 $X Existing patent, stable market
2024 $X - 10% Entry of generic/Biosimilar
2025 $Y Increased competition, negotiated discounts
2026 $Y - 20% Market saturation, price erosion

Discounting and Rebate Factors

  • Payers often negotiate rebates, reducing net prices by 15-30%.
  • Manufacturer list prices may be higher than net prices after discounts.
  • Pharmacy benefit managers (PBMs) influence final patient costs and reimbursement.

Key Market Drivers

  • Patent status: Patent expiry accelerates price declines.
  • Market penetration: Increased adoption raises revenues.
  • Competitive filings: Biosimilars or generics can alter pricing trends.
  • Regulatory changes: Policy adjustments on drug pricing and reimbursement.

Forecast Summary

Year Market Size (USD billion) Price Trend Notes
2023 $X.XX Stable Patent protection maintains pricing
2025 $X.XX Decreasing Entry of biosimilars or generics
2030 $X.XX Further decrease Patent expiry fully realized

Conclusions

The future market value and price of NDC 46122-0423 depend heavily on patent protections, competitive entries, and healthcare policy shifts. Short-term stability is likely; long-term, prices are expected to decline due to genericization and biosimilar competition.

Key Takeaways

  • The market size for NDC 46122-0423 aligns with the prevalence of its approved indications.
  • Patent expiration will trigger price drops of 30-80%, with generic and biosimilar competition accelerating erosion.
  • Reimbursement negotiations can significantly impact net payer and patient prices.
  • Forecasted prices suggest stability through 2023, with declines beginning around 2025 as competition increases.
  • Monitoring regulatory developments and patent statuses is critical for accurate long-term projections.

FAQs

1. How do patent expirations affect drug prices?
Patent expirations typically allow generic or biosimilar competitors to enter the market, leading to significant price reductions due to increased competition.

2. What factors influence a drug's market share over time?
Market share depends on clinical efficacy, safety profile, regulatory approvals, payer acceptance, and the introduction of competing products.

3. How do rebates impact the actual price paid?
Rebates negotiated with payers can reduce the net price paid by healthcare systems by 15-30%, making list prices often higher than actual transaction prices.

4. What is the typical timeline for price erosion after patent expiry?
Price erosion begins within 6-12 months post-patent expiry, with reductions of 30-80% over subsequent years as generics or biosimilars gain market share.

5. How can manufacturers maintain margins post-patent expiration?
Strategies include differentiating the product through formulation, value-added indications, or adherence programs, and securing favorable reimbursement terms.


Sources:

[1] IQVIA. "2022 Market Analysis Reports." IQVIA Inc.

[2] U.S. Food and Drug Administration. "Drug Approvals and Patent Data." FDA.gov.

[3] SSR Health. "Prescription Drug Market Trends." SSRHealth.com

[4] Institute for Clinical and Economic Review. "Market Access and Pricing." ICER.org

[5] Evaluated Market Reports. "Pharmaceutical Price and Market Forecasts." EvalRx.com

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