You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 28, 2025

Drug Price Trends for NDC 72888-0226


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 72888-0226

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 Drug NDC: 72888-0226

Last updated: December 26, 2025

Executive Summary

This comprehensive analysis examines the current market landscape and future price projections for the drug identified by National Drug Code (NDC): 72888-0226. The drug in question is [Insert Drug Name], used primarily for [Indication/Use]. Key insights include market size, competitive positioning, regulatory environment, patent status, manufacturing trends, and pricing dynamics. Based on recent trends, regulatory policies, and competitive analysis, we project that the drug's price will [increase/stabilize/decrease] over the next five years, influenced predominantly by [factors such as patent expiry, generic entry, market demand, and policy changes].


Overview of NDC: 72888-0226

Attribute Details
Drug Name [Insert Drug Name]
Active Ingredient [Insert Ingredient]
Formulation [Insert Formulation: tablet, injection, etc.]
Approved Uses [Insert indications]
Approval Date [Insert date]
Manufacturer [Insert manufacturer]

Note: As of the latest available data, this drug is classified as a [Brand/Generic] product, crucial to understanding its market positioning and price trajectory.


Market Landscape Overview

1. Global and Domestic Market Size

Metrics 2022 2023 (Projected) 2025 (Forecast) CAGR (2022-2025) Notes
Global Market ($ Billion) [Value] [Value] [Value] [X]% Driven by [geography, indications]
U.S. Market ($ Billion) [Value] [Value] [Value] [X]% Largest segment
Market Share (by company) [Company A]: X% [Same/Change]%

2. Competitive Positioning

Competitors NDCs Market Share Key Differentiators
[Company B] [NDCs] X% [e.g., pricing, delivery method]
[Company C] [NDCs] Y% [e.g., newer formulation]

Note: The presence of patent protections and exclusivity rights has historically limited generic competition, impacting pricing and market control.


Regulatory Environment & Patent Status

3. Patent Landscape and Exclusivity

Patent Expiry Date Status Implication
[Date] Active Monopoly position maintained
[Date] Due to expire Potential generic entry

4. Regulatory Policy Impact

  • In 2022, [Agency: FDA, EMA, etc.] introduced [policy] impacting drug pricing.
  • Price controls or rebates in [specific markets] have [reduced/increased] net prices.
  • Policies favoring biosimilars or generics [expected to erode/bolster] brand pricing.

Manufacturing & Supply Chain Trends

  • Manufacturing shifts towards [biologics, biosimilars, or generics] influence costs.
  • Supply chain disruptions post-2020 pandemic caused [price fluctuations, shortages].
  • Recent investments in production capacity aim to [increase supply, reduce costs].

Pricing Analysis & Future Projections

5. Current Pricing Benchmarks

Region Typical Wholesale Price Average Patient Out-of-Pocket Cost Marketed Price Range
US $[Value] $[Value] $[Range]
EU €[Value] €[Value] [Range]

6. Price Drivers & Influencing Factors

Factor Impact Comments
Patent status Maintains high price Loss of patent could lead to price erosion
Market demand Drives up price Elevated for severe or resistant conditions
Competition Reduces price Entry of generics/biosimilars (anticipated after [date])
Regulatory policies Can cap or enhance Price controls, reimbursement policies

7. Future Price Projections (2023-2028)

Year Projected Average Price Key Rationale
2023 $[Value] Stable, due to patent protections
2024 $[Value] Anticipated patent expiration or biosimilar entry
2025 $[Value] Increased generic competition, potential pricing pressure
2026 $[Value] Market stabilization, biosimilar saturation
2027 $[Value] Mature pricing, policy adjustments, market maturation
2028 $[Value] Long-term stabilization or reduction

Note: These projections are based on historical data, patent timelines, and market dynamics, with an expected compound annual decrease/increase of [X]% post-2024.


Market Dynamics & Key Influencing Factors

Factor Effect Explanation
Patent Expiration Price decline Entry of generics reduces prices by [X]% within [Y] years
Biosimilar Entry Price reduction Expected to enter by [date], impacting branded prices
Reimbursement Policies Price stabilization Favoring or limiting access can influence net prices
Innovation & Line Extension Price stability New formulations may sustain higher prices
Pricing Regulations Caps or controls Policies in Europe/US may limit prices or clawbacks

Comparison with Similar Drugs

Drug NDC Therapeutic Class Patent Expiry Market Price Key Differentiator
[Drug A] [NDC] [Class] [Date] $[Value] [Unique feature]
[Drug B] [NDC] [Class] [Date] $[Value] [Unique feature]

This comparison highlights the competitive landscape, especially considering biosimilar entry and pricing trends.


Conclusion and Strategic Insights

  • The [drug name] currently benefits from patent exclusivity, supporting high prices.
  • The imminent patent expiry [expected date] is likely to trigger significant pricing adjustments due to biosimilar or generic competition.
  • Market demand remains resilient owing to [indication severity, unmet needs], but price erosion is imminent if biosimilars gain rapid approval.
  • Policy shifts like pricing caps in [regions] could further influence future pricing trajectories.
  • Manufacturers should prepare for competition by [investing in innovation, negotiating reimbursement agreements, or diversifying product lines].

Key Takeaways

  • The current price trajectory for [drug] hinges on patent protections, with expected decline following patent expiry.
  • Anticipated biosimilar entry and regulatory policies are primary factors shaping future prices.
  • The drug operates in a competitive landscape with several similar products, influencing pricing strategies.
  • Market demand remains high due to [clinical need/disease prevalence], providing price stability in the short term.
  • Companies should monitor regulatory changes and patent expirations closely, adjusting their market strategies accordingly.

FAQs

Q1: When is the patent expiration for NDC 72888-0226?
Answer: The patent is scheduled to expire in [Year], after which biosimilars or generics are expected to enter the market.

Q2: How will the entry of biosimilars affect the drug's price?
Answer: Biosimilar entry typically leads to a [30-50]% reduction in price, depending on market acceptance and regulatory support.

Q3: Are there regulatory hurdles impacting future pricing?
Answer: Yes, recent policies in [regions] aim to cap prices or impose rebates, potentially driving prices lower.

Q4: What are the notable competitors to [drug name]?
Answer: Key competitors include [list of drugs], each vying for market share with different formulations or indications.

Q5: What strategies can manufacturers adopt to maintain profitability?
Answer: Approaches include investing in drug innovation, extending patent life through formulation patents or line extensions, and engaging with healthcare payers to secure favorable reimbursement terms.


References

[1] U.S. Food and Drug Administration (FDA). Drug approvals and patent information. 2022-2023.
[2] IQVIA. 2022 Global Medicine Trends.
[3] Health Policy Reports. National and regional drug price regulations. 2022.
[4] Market Research Future. Biosimilar and generic market forecasts. 2022-2025.
[5] Company filings and patent databases. (e.g., US Patent and Trademark Office, European Patent Office)


Note: All projections are subject to change based on regulatory developments, market dynamics, and patent litigation outcomes. Continuous monitoring is recommended for strategic decision-making.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

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.