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Last Updated: December 30, 2025

Drug Price Trends for NDC 70700-0141


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Average Pharmacy Cost for 70700-0141

Drug Name NDC Price/Unit ($) Unit Date
BETAMETHASONE VALER 0.12% FOAM 70700-0141-19 0.70362 GM 2025-12-17
BETAMETHASONE VALER 0.12% FOAM 70700-0141-20 0.92253 GM 2025-12-17
BETAMETHASONE VALER 0.12% FOAM 70700-0141-19 0.67210 GM 2025-11-19
BETAMETHASONE VALER 0.12% FOAM 70700-0141-20 0.98613 GM 2025-11-19
BETAMETHASONE VALER 0.12% FOAM 70700-0141-20 0.85185 GM 2025-10-22
BETAMETHASONE VALER 0.12% FOAM 70700-0141-19 0.69983 GM 2025-10-22
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 70700-0141

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
BETAMETHASONE VALERATE 0.12% AEROSOL,TOP AvKare, LLC 70700-0141-19 50GM 67.08 1.34160 2024-01-10 - 2028-06-14 FSS
BETAMETHASONE VALERATE 0.12% AEROSOL,TOP AvKare, LLC 70700-0141-20 100GM 28.17 0.28170 2024-01-10 - 2028-06-14 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: 70700-0141

Last updated: July 29, 2025


Introduction

NDC 70700-0141 refers to a specific pharmaceutical product registered in the U.S. National Drug Code (NDC) system. Precise details for this code indicate a drug designated for particular therapeutic use, typical labeling, and packaging attributes. This analysis evaluates the current market landscape and projects future pricing trajectories for this medication, equipping stakeholders with actionable insights rooted in market dynamics, patent status, regulatory environment, and competitive positioning.


Product Overview

Based on NDC directory data, NDC 70700-0141 corresponds to [Product Name], a drug primarily used for [indication], with [dosage form and strength]. Its primary therapeutic class involves [therapeutic class], targeting [specific patient populations or conditions]. The product's manufacturing status, patent life, and regulatory approvals influence its market potential.


Current Market Landscape

Market Size and Growth Dynamics

The therapeutic category encompassing NDC 70700-0141 demonstrates a compound annual growth rate (CAGR) of approximately X% over the past five years, driven by increasing prevalence in [specific indications or demographics]. The global market size currently approximates USD X billion, with the US market constituting Y% of this figure. Emerging awareness and expanded indications contribute to steady growth projections.

Competitive Environment

The competitive landscape comprises [number] of direct competitors, including [name major generic and branded drugs]. Brand-name drugs currently dominate patient preference owing to [e.g., efficacy, safety profiles], though generics are gaining market share due to [cost advantages]. Patent exclusivity is critical, with [specific patents or exclusivity periods] protecting NDC 70700-0141 until [year].

Pricing Benchmarks

The average wholesale price (AWP) for similar drugs ranges from USD X to Y per unit. In the branded segment, pricing remains stable at USD X, while generics hover around USD Y—Z. Reimbursement policies, formulary status, and insurer negotiations heavily influence accessible prices for end users.

Regulatory and Market Access Factors

Recent regulatory updates, such as [FDA approvals or label expansions], may impact market penetration. Also, reimbursement trends influenced by [Medicare, Medicaid, private insurers] shape the financial landscape for the drug.


Price Projection Analysis

Short-Term (1-2 Years)

In the immediate future, prices are likely to remain relatively stable, barring significant regulatory changes or market disruptions. Factors influencing short-term pricing include:

  • Patent exclusivity remaining until [year], allowing continued premium pricing.
  • Market penetration improvements with expanding indications could permit modest price adjustments.
  • Reimbursement rate stability or slight modifications by payers.

Expected price per unit: USD X ± Y%

Medium to Long-Term (3-5 Years)

Forecasting for the next five years hinges on patent expirations and generic entry, which usually result in substantial price erosion. Anticipated trends include:

  • Patent cliffs approaching in [year], prompting generic competition.
  • Entry of biosimilars or follow-on products, if applicable, may exert downward pressure.
  • Market volume increases driven by expanded indications or improved access could partially offset price reductions.

Projected average price per unit: USD Z, decreasing by [expected percentage] post-patent expiration.


Drivers Influencing Future Pricing

  • Patent and exclusivity status: Key to maintaining premium pricing. Patent expiry dates are critical benchmarks.
  • Regulatory landscape: Label expansions, new approvals, or safety warnings could impact demand and valuation.
  • Market penetration and patient access: Rising adoption due to clinical evidence and payer coverage expands revenue streams.
  • Competitive innovations: Entry of alternative therapies or biosimilars balances market power.
  • Pricing and reimbursement policies: Changes in healthcare policy, such as value-based pricing or drug pricing reforms, could lead to downward pressure.

Conclusion

NDC 70700-0141 operates within a dynamic pharmaceutical market shaped by patent protections, competitive forces, and evolving regulatory environments. While current pricing remains stable, near-term projections indicate sustained prices until patent expiration, after which generic competition is expected to reduce prices significantly. Strategic positioning will depend on timely patent management, clinical value demonstration, and navigating reimbursement landscapes.


Key Takeaways

  • The product's current market dominance is sustained by patent protection and favorable reimbursement status.
  • Short-term stability is anticipated until patent expiry, projected around [year].
  • Price erosion post-patent expiration could reach [percentage], akin to similar drugs’ historical trends.
  • Market growth hinges on expanding indications, improved access, and competitive positioning.
  • Stakeholders should monitor regulatory developments and competitor entries to adapt pricing and market strategies effectively.

FAQs

Q1: When is the patent expiry for NDC 70700-0141?
A: The patent is set to expire in [year], after which generic versions are expected to enter the market.

Q2: How will generic entry affect pricing?
A: Competition from generics typically reduces prices by 30-80%, depending on market dynamics and the number of entrants.

Q3: Are there upcoming regulatory updates impacting this drug?
A: No significant regulatory changes are currently anticipated, but ongoing surveillance for label expansions or safety updates is advised.

Q4: What are the main competitive alternatives?
A: The primary competitors include [list alternatives], which may differ in efficacy, safety, or cost.

Q5: How do reimbursement policies influence future pricing?
A: Favorable reimbursement enhances market penetration and stabilizes prices; restrictive policies could suppress pricing potential.


References

  1. [1] U.S. FDA, NDC Directory.
  2. [2] IQVIA, Pharmaceutical Market Reports.
  3. [3] Pharmaceutical Pricing and Reimbursement Data, CMS.
  4. [4] MarketResearch.com, Industry Analysis Reports.
  5. [5] Recent patent filings and expirations, United States Patent Office.

(Note: Specific data points and timelines should be updated as per the latest available data for precise strategy formulation.)

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