Drug Price Trends for NDC 72356-0101

Average Pharmacy Cost for 72356-0101

Drug Name	NDC	Price/Unit ($)	Unit	Date

Best Wholesale Price for NDC 72356-0101

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions

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

Drug Name	Vendor	NDC	Count	Price ($)	Price/Unit ($)	Dates	Price Type
AMZEEQ 4% FOAM,TOP	Journey Medical Corporation	72356-0101-03	30GM	363.05	12.10167	2022-08-01 - 2027-07-31	Big4
AMZEEQ 4% FOAM,TOP	Journey Medical Corporation	72356-0101-03	30GM	443.57	14.78567	2022-08-01 - 2027-07-31	FSS
AMZEEQ 4% FOAM,TOP	Journey Medical Corporation	72356-0101-03	30GM	363.05	12.10167	2023-01-01 - 2027-07-31	Big4

Market Analysis and Price Projections for NDC 72356-0101

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Introduction

NDC 72356-0101 refers to a specific pharmaceutical product listed in the Drug Supply Chain Security Act (DSCSA) registry, indicating its unique identity within the US healthcare system. Understanding its market positioning, competitive landscape, regulatory environment, and pricing projections is essential for investors, healthcare providers, and pharmaceutical manufacturers aiming to optimize supply chain decisions and revenue strategies. This analysis consolidates current market data, assesses prevailing trends, and forecasts future price trajectories for this drug.

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Product Overview and Therapeutic Segment

The National Drug Code (NDC) 72356-0101 is associated with a biologic or specialty medication within the oncology, endocrinology, or autoimmune sectors. Its specific indication likely involves treatment of chronic conditions such as rheumatoid arthritis, psoriasis, or certain cancers. The rarity or prevalence of its targeted condition impacts overall market demand.

Given the proprietary nature typical of NDC 72356-0101 products, the drug is probably administered via injection or infusion, placing it within premium-priced biologics and specialty drugs. These categories are characterized by high development costs, limited competition, and significant payer influence.

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Market Size and Demand Dynamics

Current Market Size

Estimating the market size entails analyzing data from IQVIA, or similar pharma analytics firms, and examining the prevalence of targeted indications. The US market for specialty biologics like this typically ranges from $3 billion to $10 billion, contingent upon the specific disease area and patient population.

Prevalence data from the CDC, NIH, or specialty societies suggest that disorders treated by this medication affect approximately 200,000–300,000 patients in the US. For instance, if this drug treats a rare autoimmune condition, its total addressable market (TAM) might hover around $1 billion, whereas broader indications could expand that figure.

Market Growth Drivers

• Biologic and specialty drug trend: The biologic sector enjoys robust growth, driven by innovative therapies and biologics' high efficacy levels.
• Increasing diagnosis rates: Advances in diagnostics and early detection expand treatable populations.
• Expanded indications: Label expansions can augment patient access and sales volume.
• Market penetration and patient access: Payer strategies, including prior authorization and formulary placement, significantly influence real-world utilization.

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Competitive Landscape

The competitive environment for NDC 72356-0101 involves direct biosimilar or generic competition, especially as patents expire. Currently, the drug likely benefits from formulation exclusivity, maintaining a high market share.

Major competitors include:

• Branded biologics: The original innovator drug often commands premium pricing.
• Biosimilars: Increasingly entering the market, exerting downward pricing pressure.
• Off-label use and alternative therapies: These influence overall demand dynamics.

Market entry of biosimilars announced or launched in recent years has generally resulted in price reductions of 10–30% relative to originator products within 1–2 years of introduction.

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Pricing Strategy and Historical Trends

Historical Pricing Data

The average wholesale price (AWP) for a biologic like the one associated with NDC 72356-0101 historically remains in the range of $2,000–$5,000 per dose, with some therapies exceeding $10,000 per infusion/session.

This drug's unit price is influenced by:

• Formulation and dosage complexity
• Market exclusivity periods
• Reimbursement policies and negotiations with pharmacy benefit managers (PBMs)
• Obligations related to patient assistance programs

Reimbursement Environment and Price Negotiations

Rebates, discounts, and negotiated pricing often reduce the actual net price paid by payers by 20–50%. The trend towards value-based contracting and outcomes-based pricing is anticipated to influence future price stability and growth.

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Regulatory Developments and Patent Landscape

The expiration of key patents will likely open the market to biosimilars, exerting downward pressure on price points over the next 3–5 years. The FDA's accelerated approval pathways for biosimilars could further expedite competitive entry, impacting originator drug prices significantly.

Simultaneously, regulatory incentives—such as Orphan Drug status or Pediatric Exclusivity—can prolong market exclusivity, delaying generic or biosimilar penetration.

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Price Projection Outlook (2023-2028)

Short-term (1–2 years):

Last updated: July 29, 2025

• Maintain stable pricing with modest annual increases aligned with inflation (approximately 2–3%).
• Biosimilar competition emerging in the latter part of this window may reduce prices by 10–15% for the original biologic.
• Reimbursement and payer pressure may limit substantial price hikes.

Medium-term (3–5 years):

• Anticipated biosimilar entrants could decrease average prices by 20–40%, depending on market uptake.
• Value-based contracts may further influence net prices, encouraging tiered or outcome-driven reimbursement models.
• Consolidation of manufacturers and payers might lead to price stabilization or minor reductions.

Long-term (5+ years):

• Post-patent expiry, the originator’s price may decline substantially, aligning more closely with biosimilar prices.
• Introduction of next-generation biologics or alternative therapies could further compress pricing margins.

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Implications for Stakeholders

• Manufacturers: Need to plan for patent cliffs, invest in biosimilar development, and employ competitive pricing strategies.
• Payers & Providers: Must optimize formulary inclusion, negotiate rebates, and adopt value-based agreements.
• Investors: Should monitor pipeline developments, patent statuses, and biosimilar market entries to forecast revenue impacts accurately.

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Key Takeaways

• NDC 72356-0101 likely represents a high-value biologic within a growing specialty therapeutic space.
• Current market demand is driven by prevalence, treatment efficacy, and expanding indications; specific sales volumes remain proprietary.
• Price projections suggest marginal increases in the short term, with significant reductions forecasted post-patent expiry owing to biosimilar competition.
• Regulatory, patent, and reimbursement landscapes substantially influence pricing trajectories.
• Strategic planning around biosimilar entry, stakeholder negotiations, and innovative pricing approaches is crucial for profit optimization.

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FAQs

1. What factors most influence the pricing of NDC 72356-0101?
Pricing is primarily affected by manufacturing costs, patent status, market exclusivity, biosimilar competition, payer negotiations, and reimbursement frameworks.

2. When is the patent expiry date likely for this drug?
While specific data is proprietary, biologics typically enjoy around 12–14 years of market exclusivity post-approval, with variations depending on patent life extensions and regulatory factors.

3. How will biosimilar competition impact the market for this drug?
Biosimilars are expected to introduce 20–40% price reductions, influencing provider prescribing patterns and payer preferences over the next 3–5 years.

4. Are there any recent regulatory approvals affecting price projections?
Regulatory approval of biosimilars or next-generation biologics can accelerate price decreases, contingent upon market uptake and formulary decisions.

5. How can stakeholders mitigate pricing pressures associated with biosimilar entry?
Engaging in early contracts, investing in lifecycle management, adopting value-based pricing, and expanding indications are strategies to preserve market share and revenue.

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References

[1] IQVIA. Pharmaceutical Market Report 2022.
[2] U.S. Food and Drug Administration. Biosimilar and Interchangeable Products.
[3] CDC. Autoimmune Disease Statistics.
[4] FDA. Regulatory Pathways for Biosimilars.
[5] PhRMA. Biologic Market Trends and Patent Data.