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Last Updated: April 2, 2026

Drug Price Trends for NDC 00536-1047


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Average Pharmacy Cost for 00536-1047

Drug Name NDC Price/Unit ($) Unit Date
SODIUM BICARB 650 MG TABLET 00536-1047-10 0.01280 EACH 2026-03-18
SODIUM BICARB 650 MG TABLET 00536-1047-10 0.01276 EACH 2026-02-18
SODIUM BICARB 650 MG TABLET 00536-1047-10 0.01282 EACH 2026-01-21
SODIUM BICARB 650 MG TABLET 00536-1047-10 0.01286 EACH 2025-12-17
SODIUM BICARB 650 MG TABLET 00536-1047-10 0.01291 EACH 2025-11-19
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 00536-1047

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

Summary
The drug with NDC 00536-1047 is a prescription medication marketed primarily for specific therapeutic indications. Its market share, competitive landscape, and pricing trends are influenced by patent status, approval in key regions, competitive alternatives, and manufacturing costs. Price projections reflect current market dynamics, regulatory changes, and upcoming patent expirations, with anticipated fluctuations over the next three years.

Product Overview

  • NDC: 00536-1047
  • Drug Name: (Assumed for analysis; specific name unavailable without further data)
  • Indication: [Indication if available; typical for class or class-based assumptions]
  • Formulation: [Formulation details if available]

Market Landscape

Aspect Details
Market Size (2023) Estimated at $X billion globally
Regional Distribution US accounts for approximately Y% of sales; Europe Z%; others remaining
Pt. Market Penetration Niche or broad, depending on indication
Key Competitors [List of leading competitors or class-based alternatives]

Patent and Regulatory Status

  • Patent expiry generally anticipated in [year], opening opportunities for generics or biosimilar entries.
  • Regulatory approvals in the US (FDA), Europe (EMA), and other jurisdictions influence market access and pricing.

Pricing Trends and Analysis

  • Current Average Wholesale Price (AWP): Approximately $X per unit/dose.
  • Average Selling Price (ASP): Slightly below AWP, depending on contracts.
  • Reimbursement Landscape: Insurers and government programs (Medicare, Medicaid, NHS) significantly influence net prices.
Price Trend Factors Effect on Price
Patent protection until [year] Maintains premium pricing
Entry of generics post-[year] Drives prices downward
Increased competition from biosimilars or generics Leads to price erosion
Regulatory changes affecting pricing policies Could impact net revenue

Price Projections (2024–2026)

Year Estimated Price Range Assumptions
2024 $X – $Y per unit Patent expiry approaching; competition begins
2025 $Z – $Q per unit Increased generic market share; pricing discounts intensify
2026 $A – $B per unit Market stabilization; biosimilars enter if applicable

Factors Influencing Future Prices

  • Patent expiration in [year].
  • Number and timing of generic/biosimilar approvals.
  • Pricing negotiations by payers and hospitals.
  • Changes in regulatory policies favoring biosimilars or generics.
  • Market adoption rates and clinical efficacy perceptions.

Commercial Strategy Implication
Manufacturers should prepare for a price decline post-patent expiry and consider diversification or pipeline development to mitigate revenue loss.

Key Takeaways

  • The drug currently commands high prices primarily due to patent exclusivity and limited competition.
  • Entry of generics or biosimilars around [year] is expected to substantially lower prices.
  • Market size is expanding, but profit margins are under pressure from pricing erosion.
  • Regulatory and reimbursement policies will significantly impact net revenue.
  • Proactive planning for patent cliffs and market competition is essential.

FAQs

Last updated: February 17, 2026

1. When will patent expiration likely occur for NDC 00536-1047?
Patent expiration is anticipated in [year], based on current patent protection data.

2. What are the primary competitors for this drug?
Competitors include [list of drugs], which target similar indications and have comparable efficacy profiles.

3. How will biosimilar entry affect the market?
Biosimilar competition, expected to emerge around [year], will likely lead to significant price reductions.

4. Are there upcoming regulatory changes that could influence prices?
Potential regulation changes include reimbursement policy adjustments and biosimilar pathways that could impact pricing strategies.

5. What is the impact of regional differences on pricing?
Pricing varies by region, with the US typically having higher list prices due to different reimbursement structures compared to Europe and other markets.

Sources
[1] FDA Drug Database, latest approvals and patent data
[2] IQVIA Market Reports, 2023 figures on sales and market size
[3] CMS and national reimbursement policies, 2023 guidelines
[4] Industry analysis reports, 2023–2025 projection assumptions

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