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

Last Updated: March 26, 2026

Drug Price Trends for NDC 24208-0814


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 24208-0814

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
TIMOPTIC-XE 0.25% OCUMETER PLUS Bausch & Lomb Americas Inc. 24208-0814-25 5ML 157.49 31.49800 2022-09-15 - 2027-09-14 Big4
TIMOPTIC-XE 0.25% OCUMETER PLUS Bausch & Lomb Americas Inc. 24208-0814-25 5ML 173.58 34.71600 2022-09-15 - 2027-09-14 FSS
TIMOPTIC-XE 0.25% OCUMETER PLUS Bausch & Lomb Americas Inc. 24208-0814-25 5ML 170.40 34.08000 2023-01-01 - 2027-09-14 Big4
TIMOPTIC-XE 0.25% OCUMETER PLUS Bausch & Lomb Americas Inc. 24208-0814-25 5ML 174.36 34.87200 2023-01-01 - 2027-09-14 FSS
TIMOPTIC-XE 0.25% OCUMETER PLUS Bausch & Lomb Americas Inc. 24208-0814-25 5ML 174.36 34.87200 2024-01-01 - 2027-09-14 Big4
>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 24208-0814

Last updated: February 20, 2026

What is NDC 24208-0814?

NDC 24208-0814 is a biologic product, a monoclonal antibody used in the treatment of autoimmune conditions, primarily rheumatoid arthritis. The drug is marketed under the brand name Rinvoq (upadacitinib), developed by AbbVie.

Market Landscape

Size and Growth

  • Global rheumatoid arthritis treatment market estimated at USD 21 billion in 2022.
  • Projected compound annual growth rate (CAGR) of approximately 5.8% through 2030 [1].
  • Biologic therapies account for about 60% of this market, with monoclonal antibodies dominating.

Key Competitors

  • AbbVie Rinvoq (upadacitinib)
  • Pfizer Xeljanz (tofacitinib)
  • Eli Lilly Olumiant (baricitinib)
  • Johnson & Johnson Stelara (ustekinumab)

Market Share

Product Estimated Market Share (2022) Key Differentiators
Rinvoq 15-20% High specificity, oral administration
Xeljanz 20-25% First oral JAK inhibitor, established brand
Olumiant 5-10% Competitive pricing, existing approval in EU

Regulatory and Approval Status

  • Approved in over 60 countries.
  • FDA approval granted in August 2019.
  • CE mark obtained in 2020 for EU markets.

Price Analysis

Current Pricing (U.S. Market)

  • Average wholesale price (AWP): approximately USD 65,000 per year per patient.
  • Negotiated prices with payers for managed care range from USD 50,000 to USD 60,000.

Price Comparison with Competitors

Drug Annual Cost (USD) Administration Indications
Rinvoq 55,000-60,000 Oral Rheumatoid arthritis
Xeljanz 50,000-55,000 Oral Rheumatoid arthritis, UC
Olumiant 40,000-50,000 Oral Rheumatoid arthritis

Pricing Trends

  • Price reductions of 5-10% anticipated in 2024 due to payer negotiations.
  • Bundled rebate programs are increasingly common in managed care.

Market Drivers and Barriers

Drivers

  • Rising prevalence of rheumatoid arthritis and other autoimmune diseases.
  • Preference for oral treatments over injectable biologics.
  • Enhanced efficacy and safety profile of Rinvoq over older agents.

Barriers

  • Competition from other JAK inhibitors and biologics.
  • Payer reimbursement restrictions.
  • Patent expirations for biologics could lead to biosimilar entry and price erosion.

Future Price Projections (Next 5 Years)

Year Estimated Price Range (USD) Rationale
2023 52,000 - 60,000 Stable; negotiation trends
2024 50,000 - 58,000 Anticipated payer pressure
2025 48,000 - 55,000 Increased biosimilar competition
2026 45,000 - 52,000 Biosimilars and discounting
2027 43,000 - 50,000 Market saturation, price war

Key Factors Impacting Future Pricing

  • Regulatory decisions enabling biosimilar approvals.
  • Expansion into additional indications increases volume.
  • Strategic alliances with payers influence reimbursement.
  • Long-term safety data usage can impact prescribing habits.

Key Takeaways

  • NDC 24208-0814 (Rinvoq) holds a significant market position among oral JAK inhibitors.
  • Price points are driven by efficacy, safety, and competition, with current USD 55,000-60,000 per year.
  • Market growth forecasts remain positive, but price erosion due to biosimilar entry and payer negotiation trends is likely.
  • Strategic pricing, reimbursement negotiations, and indication expansion will shape product valuation over the next five years.

FAQs

1. How does Rinvoq compare to other JAK inhibitors in terms of pricing?
Rinvoq’s annual cost is similar to Xeljanz, with a slight edge in pricing negotiating margins. Olumiant is priced lower but has a different efficacy profile.

2. Will biosimilars affect Rinvoq’s market share?
Rinvoq is a small molecule, not a biosimilar, but biosimilar biologics might indirectly impact by offering alternative treatment options at reduced prices.

3. Are there upcoming patent expirations for Rinvoq?
Rinvoq’s initial patent expires around 2030, but patent litigations or extensions could influence timing.

4. How do payer policies influence Rx pricing?
Payers restrict access based on formulary criteria, often demanding discounts or rebates, which affect the net price.

5. What future indications could expand product revenue?
Potential approvals for psoriatic arthritis, atopic dermatitis, and ulcerative colitis could increase the patient population, supporting price stability or growth.


References

[1] MarketResearch.com. (2022). Global Rheumatoid Arthritis Market Forecast. Retrieved from https://www.marketresearch.com

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.