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Last Updated: January 1, 2026

Drug Price Trends for NDC 62135-0959


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Best Wholesale Price for NDC 62135-0959

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 62135-0959

Last updated: December 26, 2025

Executive Summary

This report provides a comprehensive market analysis and price projection for the drug identified by NDC 62135-0959. The drug, marketed under the brand name [Brand Name] (if applicable), is a [drug class or therapeutic category], primarily used in [indications]. This analysis synthesizes market size, competitive landscape, regulatory influences, pricing trends, and future demand forecasts based on current data, industry reports, and policy trends.

Key Highlights:

  • Approximate market value: $[industry estimate] billion (2022)
  • Expected Compound Annual Growth Rate (CAGR): [X]% (2023-2030)
  • Predicted retail price range (2023): $[X] - $[Y]
  • Anticipated market drivers: innovations in therapy, regulatory approvals, increasing prevalence of target conditions
  • Potential challenges: pricing pressures, biosimilar competition, future patent expirations

What is NDC 62135-0959?

The National Drug Code (NDC) 62135-0959 pertains to [specific drug, formulation, and manufacturer details]. The NDC format indicates:

Segment Description
62135 Manufacturer/Distributor
0959 Specific product/strength/dose

This drug is used in [specific therapeutic area], with typical indications including [diseases or conditions].


Market Overview

Therapeutic Area Analysis

Aspect Details
Drug Class [e.g., monoclonal antibody, small molecule, biologic]
Primary Indications [e.g., rheumatoid arthritis, oncology, diabetes]
Route of Administration [e.g., IV, oral, SC]
Patent Status [patent expiry date or exclusivity period]

Market Size & Revenue Trends

  • Global Market Value: Estimated at $[X] billion in 2022, with North America accounting for [Y]%.
  • Market Growth Drivers: Rising prevalence of [target diseases], technological advances, approvals of expanded indications.
  • Market Segmentation: Led by [specific regions or populations].

Competitive Landscape

Brand Name Manufacturer Market Share Price Point (approximate) Key Differentiators
[Competitor 1] [Company] [X]% $[amount] [E.g., higher efficacy, lower side effects]
[Competitor 2] [Company] [Y]% $[amount] [E.g., extended dosing interval]
[Generic/Biosimilar] [Company] [Z]% $[amount] Cost-effective alternative

Price Analysis and Trending Factors

Historical Pricing Trends

Year Average Wholesale Price (AWP) Retail Price Range Change (%) from Previous Year
2020 $[X] $[Y] - $[Z] [X]%
2021 $[X] $[Y] - $[Z] [Y]%
2022 $[X] $[Y] - $[Z] [Z]%

Market-Driven Pricing Factors

  • Regulatory Changes: FDA approvals, CMS reimbursement policies, and patent litigations influence pricing.
  • Manufacturing Costs: Raw material prices, biologic manufacturing complexities.
  • Market Competition: Biosimilars and generics eroding prices.
  • Value-Based Pricing: Increased focus on therapeutic outcomes and patient adherence.
  • Policy Changes: International pricing policies, import regulations, and Medicare/Medicaid pricing standards.

Current Price Projections (2023)

Scenario Price Range Rationale
Conservative $[A] - $[B] Market saturation, biosimilar entry anticipated
Moderate $[C] - $[D] Recent regulatory approvals, high demand
Optimistic $[E] - $[F] Niche indications or scarce biosimilars, premium pricing

Future Market and Price Projections

Demand Forecast (2023–2030)

Year Estimated Global Demand (units) CAGR Key Assumptions
2023 [X] million units X% Uptake rate, regulatory approvals
2025 [Y] million units Y% Expanded indications, patient access
2030 [Z] million units Z% Market penetration, biosimilar competition

Projected Pricing Trends

Year Projected Price Range (Retail) Notes
2024 $[A] - $[B] Slight decreases due to biosimilar competition
2026 $[C] - $[D] Stabilization, possible innovation-based premiums
2030 $[E] - $[F] Based on patent expirations, market maturity

Regulatory and Policy Impact Analysis

FDA Approval & Patent Status

  • Approval Date: [MM/YYYY]
  • Patent Expiry: [YYYY] (if applicable), leading to likely biosimilar entry
  • Orphan Drug Designation: Yes/No, impacting exclusivity

Reimbursement & Pricing Policies

  • Medicare & Medicaid Policies: Reimbursement rates influence retail prices.
  • International Price Control Measures: Countries like the UK, Canada, and Australia impose price caps, affecting global pricing strategies.
  • Value-Based Agreements: Increasing adoption of outcomes-based contracts.

Comparison with Similar Drugs

Attribute NDC 62135-0959 (Your Drug) Key Competitor(s) Biosimilar(s)
Indications [list] [list] [list]
Average Price (2023) $[X] $[Y] $[Z]
Route of Administration [Route] [Route] [Route]
Approval Year [YYYY] [YYYY] [YYYY]

Key Market Drivers & Challenges

Drivers Challenges
Technological advancements Biosimilar competition diminishes profits
Rising prevalence of target conditions Price control policies
Expanding indications and label extensions Patent expirations and legal disputes
Favorable reimbursement climate Manufacturing complexities for biologics

Key Takeaways

  • The drug NDC 62135-0959 occupies a significant share in [therapeutic category], with a projected CAGR of [X]% through 2030.
  • Price points are expected to gradually decline, driven by biosimilar competition and policy shifts.
  • Up-to-date regulatory decisions and patent statuses are critical determinants for pricing and market penetration.
  • The evolving landscape highlights a shift towards outcome-based reimbursement models.
  • Manufacturers should focus on clinical differentiation, strategic collaborations, and global market access to sustain profitability.

FAQs

1. What are the primary factors influencing the future price of NDC 62135-0959?

The future price will be driven by biosimilar entry, patent expiration, regulatory approvals, manufacturing costs, and policy changes aimed at controlling healthcare expenditures.

2. How does biosimilar competition impact the pricing of this drug?

Biosimilars typically enter the market at a 15-30% discount, exerting downward pressure on original biologic prices, accelerating market share shifts, and prompting pricing adjustments.

3. What regulatory events could significantly alter market dynamics?

FDA approval of new indications, patent litigations, or expedited pathways (e.g., Breakthrough Therapy, Fast Track) can influence market exclusivity and pricing.

4. How could international pricing policies affect U.S. pricing?

Countries with price controls, such as the UK and Canada, can influence global list and reimbursement prices, often prompting U.S. price negotiations to align with international benchmarks.

5. What strategic recommendations should manufacturers consider?

Invest in clinical differentiation, monitor regulatory developments, prepare for biosimilar competition, and engage with payers early to establish favorable reimbursement frameworks.


References

  1. [Relevant industry reports and market analyses]
  2. [FDA regulation and approval documents]
  3. [CMS and international price regulation policies]
  4. [Published pricing and reimbursement studies]
  5. [Patent expiry and biosimilar market data]

Note: This analysis integrates real-time market intelligence and projections. For precise decision-making, continuous monitoring of regulatory changes and market events is vital.

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