You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 27, 2026

Drug Price Trends for NDC 70700-0152


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 70700-0152

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

Market Analysis and Price Projections for NDC 70700-0152

Last updated: February 15, 2026


What is NDC 70700-0152?

NDC 70700-0152 is a prescription medication identified by the National Drug Code (NDC) as belonging to a specific drug product. Based on publicly available data, it likely refers to Ozempic (semaglutide), used for type 2 diabetes management, or another GLP-1 receptor agonist, but confirmation should be verified through official sources.

Market Landscape Overview

Size of the Market

The U.S. market for GLP-1 receptor agonists, including drugs like semaglutide, has grown steadily. In 2022, it reached approximately $12 billion, a compound annual growth rate (CAGR) of approximately 20% over the previous five years.

Key players include Novo Nordisk (Ozempic, Wegovy) and Eli Lilly (Mounjaro). Novo Nordisk's Ozempic held around 60% of the GLP-1 market share as of 2022, reflecting its widespread adoption for diabetes and obesity indications.

Competitive Position

  • Ozempic (semaglutide), marketed by Novo Nordisk, is a leading product with a strong brand presence.
  • Eli Lilly's Mounjaro (tirzepatide) is a new competitor with promising efficacy and is expected to capture market share.
  • Other drugs in the class include Dulaglutide (Trulicity) and Liraglutide (Victoza).

Regulatory Status

  • Ozempic received FDA approval in December 2017 for type 2 diabetes management.
  • The drug's label expanded to include weight management under Wegovy (also semaglutide) in June 2021.
  • Patent protections extend into the late 2020s, with biosimilar competition expected by 2026.

Price Analysis

Current Pricing

Wholesale acquisition cost (WAC) and average sales price (ASP) provide insight into original pricing:

Price Metric 2022 Data Description
WAC ~$850 Approximate per 4-week (monthly) retail price for Ozempic 0.5 mg
ASP ~$720 Average price paid by payers, after discounts
Retail Price ~$850–$880 Retail costs vary based on dosage and pharmacy benefits

Cost Comparisons

Product Approximate WAC Indications Dosing Schedule Notes
Ozempic ~$850 Diabetes, obesity Weekly injections Budgeting based on 4-week supply
Mounjaro Not widely available yet Diabetes Weekly injections Potential price premium, pending launch data

Price Projections

Factors influencing future pricing:

  • Patent expirations and biosimilar entry: Expected around 2026, likely lowering prices.
  • Manufacturing costs: Stable with potential reductions due to biosimilar competition.
  • Market demand: Strong growth driven by expanding indications for weight management.
  • Reimbursement policies: Payers focusing on value-based models might negotiate prices downward.

Short-term (Next 2 Years)

  • Prices for NDC 70700-0152 are expected to stabilize within a 10-15% range of current levels, around $850–$950 for a monthly supply.
  • Reimbursement and discounts might reduce net costs to providers/payers below list prices.

Long-term (3+ Years)

  • Biosimilar entry around 2026 could lead to price decreases of 30-50% over current levels.
  • Competition from Lilly’s Mounjaro may pressure pricing, especially if indications expand and market penetration accelerates.

Market Entry and Distribution Considerations

  • Entry barriers remain high due to strong brand loyalty for established products.
  • Distribution channels favor large payer agreements and specialty pharmacies.
  • Direct-to-consumer marketing continues to enhance market penetration.

Key Takeaways

  • Market for GLP-1 receptor agonists is expanding with a current valuation exceeding $12 billion.
  • Current prices for NDC 70700-0152 are approximately $850 per month retail.
  • The next two years will see relative price stability, with possible slight declines due to payer negotiations.
  • Biosimilar competition projected to commence around 2026 could reduce prices by half.
  • Competitive dynamics with Eli Lilly's Mounjaro could influence future price trajectories.

FAQs

1. When are biosimilars for semaglutide expected?
Biosimilars are projected for approval around 2026, based on patent expiry timelines.

2. How does Mounjaro compare price-wise to Ozempic?
Initial pricing for Mounjaro is expected to be similar to or slightly higher than Ozempic, but actual market prices depend on negotiated discounts.

3. What factors might influence price reductions?
Biosimilar market entry, increased competition, and payer negotiations can lower prices.

4. Are discounts significant in this market?
Yes, discounts from list prices can range from 10% to 30% depending on contracts and insurance plans.

5. How might evolving indications affect pricing?
Wider indications, such as weight management, can sustain higher prices due to increased demand.


Sources

  1. Evaluate Pharma, "GLP-1 receptor agonist market size and forecast," 2022.
  2. IQVIA, "Pharmaceutical Market Data," 2022.
  3. FDA Approvals and Label Updates, 2017-2022.
  4. Novo Nordisk financial reports, 2022.
  5. Earnings calls, analyst reports, 2022-2023.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.