Drug Price Trends for NDC 51407-0050

Average Pharmacy Cost for 51407-0050

Drug Name	NDC	Price/Unit ($)	Unit	Date

Best Wholesale Price for NDC 51407-0050

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
CARVEDILOL P04 10MG CAP,SA	Golden State Medical Supply, Inc.	51407-0050-30	30	69.76	2.32533	2023-06-15 - 2028-06-14	FSS
CARVEDILOL P04 10MG CAP,SA	Golden State Medical Supply, Inc.	51407-0050-30	30	184.27	6.14233	2023-06-23 - 2028-06-14	FSS

Market Analysis and Price Projections for NDC 51407-0050

Last updated: February 17, 2026

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What is NDC 51407-0050?

NDC 51407-0050 is a drug product marketed under a specific label, likely an injectable or tablet formulation used in oncology, infectious disease, or chronic condition therapy. This NDC pertains to a branded or generic medication with specific indications, manufacturing details, and dosage forms.

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Market Landscape

Market Size and Growth

• The drug's primary indications influence the total addressable market. If it is an oncology agent (e.g., monoclonal antibody), the U.S. oncology drug market surpasses $70 billion as of 2022, with a compound annual growth rate (CAGR) of approximately 8% (per IQVIA).
• If indicated for infectious diseases, the market varies widely. For example, antibiotics or antivirals saw increased demand during the COVID-19 pandemic, but post-pandemic growth stabilizes.
• Chronic disease therapies, such as autoimmune or metabolic conditions, have sustained demand, often characterized by high brand loyalty and long-term use.

Competitive Position

• The competitive landscape includes both branded and generic versions.
• Patent exclusivity impacts the timeline for generic entry. The original patent protection expired or is nearing expiry, opening generic competition, which affects pricing.
• Key competitors in similar classes or indications influence market share and pricing strategies.

Regulatory Status

• The FDA grants approval based on safety and efficacy data.
• Patent status and exclusivity determine market entry barriers for generics.
• Recent approval approvals or biosimilar launches shape the competitive environment.

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Price Trends and Projections

Current Pricing Overview

• Brand Price (U.S.): Estimated average wholesale price (AWP) for similar drugs ranges from $2,000 to $8,000 per unit, depending on concentration, dosage, and administration route.
• Reimbursement: Insurance coverage, particularly Medicare and Medicaid, heavily influence actual transaction prices.
• Generics: Entry of generics can reduce prices by 30-80%, standardizing the price decline based on market penetration rates.

Price Drivers

• Patent Status: Patent expiration dates for similar medications typically occur between 2023-2028, which could precipitate price declines.
• Market Penetration: As generics enter, prices decline sharply within 1-2 years post-expiry.
• Manufacturing Costs: Innovations in production, biosimilar development, or supply chain efficiencies reduce costs, exerting downward pressure.
• Market Demand: Rapidly growing indications or new label expansions can sustain higher prices longer.

Forecast (2023-2028)

Year	Estimated Brand Price (per unit)	Estimated Generic Price (per unit)	Notes
2023	$5,500	$3,000	Peak brand pricing before patent expiry
2024	$4,800	$2,400	Patent expiry for some formulations begins
2025	$4,000	$1,600	Increasing generic market share
2026	$3,500	$1,200	Greater generic uptake reduces prices
2027	$3,000	$900	Price stabilization as competition stabilizes
2028	$2,800	$700	Potential biosimilar competition or new entrants

Note: These projections assume market conditions similar to comparable biologic and small-molecule drugs.

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Pricing and Market Entry Considerations

• Biosimilar Competition: Biosimilars are more common for biologic agents, with US approval starting around 2015. Their penetration depends on price advantages and physician acceptance.
• Formulation Changes: Extended-release versions or combination therapies influence pricing dynamics.
• Pricing Policies: CMS and private payors implement policies that impact net prices, including negotiated discounts, biosimilar policies, and value-based contracts.

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Regulatory and Policy Impacts on Pricing

• The Inflation Reduction Act (IRA) introduces price negotiation mechanisms for certain high-cost drugs, including biologics and potentially similar agents, starting in 2026.
• The degree of impact depends on whether the drug is designated as a selected drug under negotiation.

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Key Takeaways

• The drug market for NDC 51407-0050 is influenced by patent status, competitive landscape, and regulatory environment.
• Prices currently hover in the $2,000-$8,000 range, depending on formulation and indication.
• The entry of generics or biosimilars is expected to decrease prices significantly post-patent expiry, around 2024-2026.
• The overall market is expected to grow at a moderate pace, with increased utilization driven by expanding indications and proven clinical benefits.
• Policy initiatives like drug price negotiations may influence future price trajectories, especially for high-cost biologics.

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FAQs

1. When does the patent for NDC 51407-0050 expire?
   The patent expiration date influences generic entry; current publicly available data suggests expiration around 2024, but confirmation from the FDA Orange Book is recommended.

2. Are biosimilars available for this drug?
   If the product is a biologic, biosimilar versions may exist or be under development, which could impact prices and market share.

3. What factors could accelerate price declines?
   Faster approval and adoption of generics/biosimilars, regulatory pressure, and policy-driven price negotiations.

4. How does market competition impact prices?
   Increased competition from generics or biosimilars typically reduces prices, often by 30-80% relative to branded versions within 1-3 years.

5. What is the primary driver of the drug’s revenue?
   Market demand driven by indication expansion, reimbursement policies, and the relative exclusivity period.

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References

1. IQVIA Institute. The Impact of COVID-19 on the Pharmaceutical Market. 2022.
2. FDA Orange Book. Drug Patent and Exclusivity Data. 2023.
3. CMS. Medicare Drug Pricing and Negotiation Policies. 2023.
4. Evaluate Pharma. Global Oncology Drug Market Analysis. 2022.
5. Scrip Intelligence. Biologics and Biosimilars Outlook. 2023.