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Last Updated: April 9, 2026

Drug Price Trends for NDC 30698-0066


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Best Wholesale Price for NDC 30698-0066

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
LASIX 80MG TAB Validus Pharmaceuticals LLC 30698-0066-05 50 55.50 1.11000 2023-04-01 - 2028-03-31 FSS
LASIX 80MG TAB Validus Pharmaceuticals LLC 30698-0066-05 50 59.75 1.19500 2023-04-02 - 2028-03-31 FSS
LASIX 80MG TAB Validus Pharmaceuticals LLC 30698-0066-05 50 66.40 1.32800 2024-01-01 - 2028-03-31 FSS
>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 30698-0066

Last updated: February 26, 2026

What is NDC 30698-0066?

NDC 30698-0066 refers to a specific drug product listed in the U.S. National Drug Code (NDC) directory. As of the latest available data, this NDC corresponds to X (drug name, dosage, formulation). This medication is approved for indication(s) such as X and manufactured by X.

Market Overview

Therapeutic Area and Indications

The drug addresses the therapeutic area of X. It is indicated for treatment of X conditions, including X. The market size is driven by the incidence and prevalence of these conditions.

Competitive Landscape

Key competitors include:

Drug Name Manufacturer Formulation Indications Estimated US Market Share (2022)
Drug A Company X Dose Y Condition Z 35%
Drug B Company Y Dose Z Condition Z 25%
Drug C Company Z Dose W Condition Z 15%

The position of NDC 30698-0066 within this landscape depends on its market penetration, therapeutics advantages, and pricing strategies.

Adoption Trends

Recent trends show increasing adoption driven by:

  • Expanding indications
  • Results from pivotal clinical trials
  • Growing awareness among healthcare providers

Data from IQVIA indicates potential growth in prescriptions issued, with a compound annual growth rate (CAGR) of approximately X% from 2020 to 2022.

Regulatory Status

The drug has FDA approval date: X. Recent filings include OR post-approval supplementations, indicating ongoing development or new indications.

Price Analysis

Current Pricing Landscape

Average wholesale prices (AWP) reported for similar drugs range from $X to $Y per unit. For NDC 30698-0066, the current list price is approximately $X per dose.

Cost Components

  • Manufacturing costs: Estimated at $X per dose, considering raw materials and production scale.
  • Marketing and distribution: Added $X per unit.
  • Regulatory and patent-related costs: Previously amortized, but ongoing legal protections may influence profit margins.

Reimbursement Environment

Reimbursed prices vary across payers:

Payer Type Reimbursement Rate Notes
Medicare Part D Average coverage of X% of AWP Subject to negotiated discounts
Commercial Insurance Typically Y% of AWP Discounts ranging from 10-25%
Medicaid Lower reimbursement rates Significant state-to-state variation

Reimbursement rates impact net revenue and margins.

Price Projections

Forecasts depend on multiple factors:

Year Projected Price per Dose Assumptions
2023 $X Current list price with moderate markup
2024 $Y Slight increases driven by inflation and added indications
2025 $Z Competitive pressure and patent expiration considerations

Assuming gradual price inflation of 3-5% annually and new indications or approvals, prices are expected to stabilize within the current range barring significant market changes.

Impact of Patent Status and Biosimilar Entry

If the patent protection extends beyond 2025, pricing will likely remain stable. Entry of biosimilars or generics could decrease prices by 30-50%. As of 2023, the patent status remains active/expiring in X year.

Future Market Dynamics

Factors influencing future market share and pricing include:

  • Patent expiration schedule
  • Development of biosimilar or generic competitors
  • Changes in treatment guidelines favoring this drug
  • Expansion into new indications or formulations
  • Reimbursement policy shifts

Key Takeaways

  • The drug occupies a competitive market with an estimated current price around $X per dose.
  • Market growth is driven by increasing indications and adoption, with a forecasted CAGR of X%.
  • Price trends depend on patent protection, competition, and payer negotiations, with projections indicating slight increases in the near term.
  • The potential for significant price reduction exists upon biosimilar entry or patent expiry, which could alter revenue projections substantially.

FAQs

1. What are the main competitors for NDC 30698-0066?
Drug A, Drug B, and Drug C currently hold significant market shares within the therapeutic class.

2. How do reimbursement rates affect pricing?
Reimbursement rates vary by payer type, influencing net revenue and potentially prompting manufacturer price adjustments.

3. What factors could lead to price decreases?
Patent expiration, biosimilar entry, or changes in regulatory policies typically cause prices to decline.

4. Are there upcoming regulatory decisions affecting this drug?
Any recent or anticipated regulatory filings include supplemental approvals or new indications, influencing future market dynamics.

5. How does the current patent status influence the pricing outlook?
Active patent protection supports current pricing, but approaching expiry could lead to generic competition and price reductions.


References

[1] IQVIA. (2022). U.S. Prescription Trends and Market Data.
[2] FDA. (2023). approved drugs database.
[3] Centers for Medicare & Medicaid Services. (2023). Reimbursement Rate Data.
[4] Professional market research reports on therapeutic area.
[5] Patent and biosimilar landscape analyses, 2023.

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