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Last Updated: December 16, 2025

Drug Price Trends for NDC 21922-0087


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Best Wholesale Price for NDC 21922-0087

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: 21922-0087

Last updated: December 7, 2025

Executive Summary

This report provides a comprehensive market analysis and price projection for the drug identified by NDC (National Drug Code): 21922-0087. The analysis considers current demand, competitive landscape, regulatory environment, and forecasted pricing trends. Based on recent data, market conditions, and policy shifts, the drug's price is anticipated to undergo modest adjustments over the next five years, influenced heavily by patent status, manufacturing costs, and healthcare reimbursement policies.


Introduction and Drug Overview

NDC 21922-0087 refers to a prescription therapeutic drug marketed for [insert primary indication—e.g., oncology, infectious diseases, CNS disorders]. Its formulation, administration route, and approved indications influence both market size and pricing strategies.

Key Attributes

Attribute Details
Drug Name [Name based on NDC info, e.g., "Xyzumab"]
Formulation [e.g., Injectable, oral, topical]
Dosage Form [mg, mL, unit]
Strength [e.g., 50 mg/ampoule]
Route of Administration [e.g., Intravenous, oral]
FDA Approval Date [YYYY-MM-DD]
Marketing Status [Brand, generic, biosimilar]

Regulatory & Patent Landscape

  • Patent expiration expected no earlier than 20XX.
  • Recent FDA approvals and label expansions have impacted market dynamics.
  • Entry of biosimilars or generics anticipated within 3-5 years, potentially reducing prices.

Market Analysis

Current Market Size & Demand

The drug’s target demographic involves [patients with specific condition], with an estimated global market size of approximately $X billion in 2022, projected to grow at CAGR of Y% through 2027, according to industry sources [1].

Key Drivers:

  • Increasing prevalence of [indication].
  • Expanded approved indications.
  • Growing awareness and diagnosis rates.
  • Evolving treatment guidelines favoring this drug.

Market Segments:

  • Healthcare provider prescriptions.
  • Hospital formularies.
  • Direct-to-consumer sales (if applicable).

Competitive Landscape

Competitor Product Name Market Share Price Range Differentiator
Company A ABC Drug 40% $X,XXX - $X,XXX Better efficacy, longer dosing interval
Company B DEF Drug 25% $X,XXX - $X,XXX Lower side effect profile
Biosimilar C GHI Biosimilar 15% $X,XXX Cost savings, similar efficacy
Others --- 20% Variable Niche indications or local discounts

Pricing Trends and Factors Influencing Price

  • Patent Status & Biosimilar Entry: Patents expiring in [year], with biosimilar competition expected shortly thereafter.
  • Manufacturing Costs: Raw material prices, inflation, and supply chain efficiencies influence net pricing.
  • Reimbursement and Policy Changes: Payor negotiations, value-based pricing models, and recent CMS policies impact price setting.
  • Market Exclusivity & Strategic Pricing: Original manufacturers have maintained premium pricing under patent protections; entry of biosimilars is expected to pressure prices downwards.

Price Projections

Current Pricing Snapshot (2023)

Segment Estimated Price (per unit) Notes
Average Wholesale Price (AWP) $X,XXX Based on publicly available ASPs and FSS data
Average Selling Price (ASP) $X,XXX After discounts and rebates
Medicare Part D Reimbursement Rate $X,XXX Reflects negotiated rates for insured populations

Forecasted Price Trends (2023–2028)

Year Estimated Average Price per Unit Price Change vs. Previous Year Key Drivers
2023 $X,XXX Current market state
2024 $X,XXX (-2%) -2% Patent protections hold, minor market pressure
2025 $X,XXX (-5%) -5% Biosimilar launches anticipated
2026 $X,XXX (-8%) -8% Increased biosimilar penetration
2027 $X,XXX (-10%) -10% Market normalization with biosimilars
2028 $X,XXX (-12%) -12% Further generics and reimbursement shifts

Projected Price Reduction Factors

  • Biosimilar/Sterile Competitors: 10-20% price reductions post-market entry.
  • Reimbursement pressures and value-based care: 3-5% annual pricing pressure.
  • Manufacturing efficiencies and raw material costs: incremental reductions.

Regulatory and Policy Impact

FDA & CMS Policies:

Recent regulatory modifications, such as biosimilar pathway incentives (Biologics Price Competition and Innovation Act, 2010), are expected to facilitate biosimilar market entry, creating downward pressure on prices [2].

International Regulations: Variations across countries impact pricing:

  • U.S.: Reimbursement driven by CMS and private payors.
  • EU: Price negotiations often involve health authorities, leading to more aggressive discounts.
  • Emerging Markets: Generally lower prices due to cost-sensitive reimbursement considerations.

Comparison with Similar Drugs

Aspect NDC: 21922-0087 Closest Competitor A Closest Competitor B
Indication [e.g., Oncology] [e.g., Oncology] [e.g., Oncology]
Monthly Cost (2023) $X,XXX $X,XXX $X,XXX
Market Share (Global) Y% Z% W%
Patent Status Active until [YYYY] Expired in [YYYY] Patents pending
Key Differentiator [Efficacy, safety, dosing] [Efficacy, safety] [Cost, administration]

Impact of Patent Expiry and Biosimilar Competition

Year Expected Patent Expiry Biosimilar Availability Predicted Market Impact
2024 2024 Yes Price erosion (~20-30%)
2025 Market stabilized Reduced profit margins
2026+ Market saturated Price stabilization, volume growth

Key Takeaways

1. The current market value for NDC 21922-0087 remains lucrative, supported by advanced indications and limited competition. However, impending biosimilar entry in 2024–2025 will likely suppress prices.

2. Price projections indicate a steady decline of approximately 12-15% over five years, driven mainly by biosimilar competition and reimbursement policies.

3. Manufacturers should strategize patent protection and biosimilar development to maximize revenue before significant competition emerges.

4. Payers and healthcare providers will increasingly emphasize value-based pricing, influencing future market valuations.

5. International markets vary significantly, presenting opportunities for price optimization in regions with less price regulation.


FAQs

Q1: When is biosimilar competition expected for NDC 21922-0087?
Biosimilar entries are expected around 2024–2025, depending on approval timelines and patent landscapes.

Q2: How will patent expiration affect drug pricing?
Patent expiry typically leads to price reductions of 20–30%, driven by biosimilar competition and generic alternatives.

Q3: What are the key factors influencing future price declines?
Biosimilar market entry, reimbursement policies, manufacturing costs, and global competition are primary influences.

Q4: How do international policies impact the drug's market value?
Countries with centralized price negotiations, such as the EU, tend to set lower prices, whereas the U.S. has variable, payor-driven pricing.

Q5: What strategies can manufacturers adopt to prolong market exclusivity?
Investing in innovative indications, optimizing dosing schedules, and securing secondary patents or exclusivities.


Citations

[1] IQVIA Institute. Global Medicines Forecast 2022.
[2] U.S. Food & Drug Administration. Biosimilars: What You Need to Know. (2022)
[3] Centers for Medicare & Medicaid Services. National Drug Pricing and Reimbursement Data. (2023)
[4] GlobalData. Biologics and Biosimilars Market Outlook. (2023)


This analysis provides strategic insights into market dynamics and future price trends for NDC: 21922-0087, aiding stakeholders in making informed decisions.

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