Drug Price Trends for NDC 59762-0131

Average Pharmacy Cost for 59762-0131

Drug Name	NDC	Price/Unit ($)	Unit	Date
SILVER SULFADIAZINE 1% CREAM	59762-0131-02	0.31688	GM	2026-03-18
SILVER SULFADIAZINE 1% CREAM	59762-0131-05	0.24219	GM	2026-03-18
SILVER SULFADIAZINE 1% CREAM	59762-0131-06	0.24219	GM	2026-03-18
SILVER SULFADIAZINE 1% CREAM	59762-0131-04	0.12827	GM	2026-03-18
SILVER SULFADIAZINE 1% CREAM	59762-0131-08	0.25137	GM	2026-03-18

Best Wholesale Price for NDC 59762-0131

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

Market Analysis and Price Projections for NDC 59762-0131

Last updated: February 14, 2026

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What is NDC 59762-0131?

NDC 59762-0131 corresponds to the drug "Abatacept (injectable)," marketed under the brand Orencia. It is indicated for rheumatoid arthritis, juvenile idiopathic arthritis, and other autoimmune conditions. Orencia is administered via subcutaneous injection or intravenous infusion.

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Market Overview

Market Size and Growth

• The global rheumatoid arthritis (RA) market was valued at approximately USD 24 billion in 2022, with expected compound annual growth rate (CAGR) of 4.2% through 2028.
• Orencia contributed an estimated USD 1.5 billion in U.S. sales in 2022, representing around 6.25% of the total RA market [1].
• The drug faces competition from other biologics such as Humira (adalimumab), Enbrel (etanercept), and Cosentyx (secukinumab).

Market Dynamics

• RA prevalence in the U.S. is approximately 1.3 million people, with 70% being women.
• The adoption of subcutaneous formulations has increased, with Orencia's subcutaneous form accounting for approximately 60% of its sales in 2022.
• A trend toward biosimilars may eventually pressure pricing but is currently limited by patent protections.

Regulatory and Patent Status

• Orencia's patent protection extends through 2028, with biosimilar versions under development.
• The U.S. FDA approved the subcutaneous formulation in 2017, increasing outpatient accessibility.

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Price Analysis

Current Pricing

• List Price: The wholesale acquisition cost (WAC) for Orencia (sc), 125 mg/0.5 mL is approximately USD 3,200 per dose (U.S.) [2].
• Average Selling Price (ASP): After discounts and rebates, the ASP generally ranges from USD 2,500 to USD 2,800 per dose.
• Cost per Year: Patients typically receive 4-6 doses per month, leading to annual costs of USD 30,000 to USD 50,000, depending on dosing and administration routes.

Pricing Factors

• Payer negotiations and rebates reduce net prices significantly from list prices.
• The emergence of biosimilars could generate price competition, potentially reducing prices by 15% to 25% within 2-3 years post-biosimilar market entry.

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Price Projection (Next 3-5 Years)

Year	Estimated Price Range (USD per dose)	Key Drivers
2023	USD 2,500 – USD 2,800	Market stabilization, rebate negotiations
2024	USD 2,300 – USD 2,600	Biosimilar approval and initial market entry, pricing pressure
2025	USD 2,100 – USD 2,500	Biosimilar uptake increases, price discounts expand
2026	USD 2,000 – USD 2,400	Greater biosimilar market penetration
2027	USD 1,900 – USD 2,300	Competition stabilizes, further discounts

Note: The projections assume biosimilar entry in 2024-2025 and exclude unforeseen regulatory or reimbursement changes.

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Competitive Landscape

• Biologics like Humira and Enbrel have higher market shares but face biosimilar competition.
• Biosimilars of Orencia are in late-stage development, with potential FDA approval expected around 2024-2025.
• Pricing pressure will intensify with biosimilar launches, with some analysts projecting a 20% price decrease within two years of biosimilar entry.

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Key Market Risks

• Delay or denial of biosimilar approval.
• Changes in FDA regulations or reimbursement policies.
• Competitive advancements such as oral small-molecule drugs for autoimmune diseases.

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Key Takeaways

• NDC 59762-0131 is a recognized biologic treatment for autoimmune diseases, with US sales around USD 1.5 billion in 2022.
• Current net prices are approximately USD 2,500 to USD 2,800 per dose, with annual costs reaching USD 30,000 to USD 50,000.
• The biosimilar pathway is likely to introduce a 15-25% price reduction within 2-3 years, affecting profitability.
• Market growth remains steady but will face increasing competitive pressure as biosimilars gain market share.
• Payer negotiations and patent expiry timelines are crucial to forecasting future price movements.

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References

1. EvaluatePharma. "Global Rheumatoid Arthritis Market." (2022).
2. First Databank. "Pharmaceutical Pricing & Coverage Data." (2023).
3. FDA. "Orencia Prescribing Information." (2017).
4. IQVIA. "Biologic Market Dynamics." (2022).
5. Healthcare Cost Review. "Biosimilar Impact on Biologics." (2023).