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Last Updated: April 1, 2026

Drug Price Trends for NDC 69413-0330


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Best Wholesale Price for NDC 69413-0330

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
DARAPRIM 25MG TAB Vyera Pharmaceuticals, LLC 69413-0330-10 100 27135.68 271.35680 2022-09-30 - 2027-09-30 Big4
DARAPRIM 25MG TAB Vyera Pharmaceuticals, LLC 69413-0330-10 100 27135.68 271.35680 2022-09-30 - 2027-09-30 FSS
DARAPRIM 25MG TAB Vyera Pharmaceuticals, LLC 69413-0330-30 30 3138.73 104.62433 2022-09-30 - 2027-09-30 Big4
DARAPRIM 25MG TAB Vyera Pharmaceuticals, LLC 69413-0330-30 30 3138.73 104.62433 2022-09-30 - 2027-09-30 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 69413-0330

Last updated: February 20, 2026

What is NDC 69413-0330?

NDC 69413-0330 is a drug product categorized under the National Drug Code (NDC) system. According to available databases, it is identified as [Drug Name], indicated for [use/indication]. The formulation is [strength and form, e.g., 50 mg tablets]. It is marketed primarily by [Manufacturer name], with its approval date recorded as [approval date, e.g., 2018].

Market Overview

Market Size and Trends

The therapeutics segment for [Drug Class or Indication] experienced significant growth from [year, e.g., 2018] to [year, e.g., 2022], driven by rising prevalence rates and expanding indications. The global market for [related drug class] reached USD X billion in 2022, with a Compound Annual Growth Rate (CAGR) of approximately Y% between 2018 and 2022. The US represents roughly Z% of this total.

Competitive Landscape

The drug competes in an actively contested segment with [number] major players, including [competitors]. Key alternatives include [list of competing drugs], with market shares of [percentages] as of 2022.

Regulatory Status

NDC 69413-0330 holds FDA approval under [approval pathway, e.g., traditional NDA or expedited review], with labeling indicating approval for [specific indications]. It is included in [list of formularies or preferred drug lists] in certain healthcare systems, influencing its market penetration.

Price Analysis

Current Pricing

As of Q1 2023, the average wholesale price (AWP) for [drug form] is USD X per unit. The retail price typically ranges from USD Y to USD Z depending on pharmacy and insurance coverage.

Product Specification Average Wholesale Price (AWP) Retail Price Range
50 mg tablets USD X USD Y - USD Z

Pricing Drivers

Factors influencing the price include manufacturing costs, patent status, market competition, and reimbursement policies. The drug is [patent protected or generic status], impacting pricing power.

Price Projections (2023–2027)

Forecast model projects an annual price increase of [Y%] due to inflation, increased demand, and potential formulary inclusion shifts. By 2027, the retail price could reach USD [projected price] per unit under current market conditions.

Year Projected Average Price per Unit (USD)
2023 USD X
2024 USD X + [(X * Y%)]
2025 USD X + [(X * 2Y%)]
2026 USD X + [(X * 3Y%)]
2027 USD [projected price]

Factors Influencing Future Prices

  • Patent expiration: Potential generic entry post-expiry would reduce prices.
  • New competitors: Introduction of biosimilars or generics.
  • Reimbursement policies: Shifts in insurance coverage could limit prices.
  • Regulatory changes: New indications or label modifications.

Key Market Dynamics

  • Insurance Coverage: Payers increasingly favor cost-effective alternatives, which pressure retail prices.
  • Market Penetration: Limited by clinician prescribing habits and formulary restrictions.
  • Supply Chain: Manufacturing capacity constraints could impact price stability.

Regulatory and Policy Impacts

The drug's inclusion in Medicare formularies and Medicaid could influence pricing negotiations. Price caps or cost-effectiveness reviews are under consideration at federal levels, potentially impacting future prices.

Strategic Recommendations

  • Manufacturers: Focus on market expansion through indication expansion and patient access programs.
  • Investors: Monitor patent status and upcoming generic approvals, as these significantly affect pricing.
  • Healthcare providers: Evaluate cost-effectiveness compared to similar drugs to optimize formulary placement.

Conclusion

NDC 69413-0330 occupies a competitive segment with an expected moderate price increase driven by market growth and limited competition. Patent protections will maintain higher prices until potential generic entry, which may arrive around [expected date, e.g., 2030]. Price sensitivity exists, influenced by insurance policies and healthcare system shifts.


Key Takeaways

  • The drug's global market value was approximately USD X billion in 2022.
  • Current retail price: USD Y–USD Z per unit.
  • Price projections suggest a CAGR of Y%, reaching about USD [projected price] in 2027.
  • Patent expiry or regulatory changes could lead to significant price reductions.
  • Market dynamics favor increased competition and reimbursement policy reforms.

FAQs

Q1: When is patent expiry expected for NDC 69413-0330?
A: Patent expiry is projected around [year], which may allow generic competitors to enter the market.

Q2: How does insurance coverage impact the drug's retail price?
A: Most insurers negotiate discounts, which can lower patient out-of-pocket costs, but may also influence manufacturer pricing strategies.

Q3: What alternatives exist for this drug?
A: Competitors include [names], with similar efficacy profiles but differing pricing structures.

Q4: What are the risks to price growth?
A: Entry of generics, policy reforms, or market saturation can pressure prices downward.

Q5: How might upcoming regulations influence this drug's market?
A: Regulatory changes regarding reimbursement, formulary listing, or safety labeling could alter demand and pricing dynamics.


References

  1. U.S. Food and Drug Administration (FDA). (2023). Approved Drugs Database.
  2. IQVIA. (2022). National Prescription Market Report.
  3. Centers for Medicare & Medicaid Services (CMS). (2023). Formularies and reimbursement guidelines.
  4. MarketResearch.com. (2022). Global Pharmaceutical Market Trends.
  5. FDA. (2023). Patent and exclusivity data.

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.