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Last Updated: April 2, 2026

Drug Price Trends for NDC 72888-0118


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Average Pharmacy Cost for 72888-0118

Drug Name NDC Price/Unit ($) Unit Date
CEVIMELINE HCL 30 MG CAPSULE 72888-0118-01 0.69784 EACH 2026-03-18
CEVIMELINE HCL 30 MG CAPSULE 72888-0118-30 0.69784 EACH 2026-03-18
CEVIMELINE HCL 30 MG CAPSULE 72888-0118-01 0.67572 EACH 2026-02-18
CEVIMELINE HCL 30 MG CAPSULE 72888-0118-30 0.67572 EACH 2026-02-18
CEVIMELINE HCL 30 MG CAPSULE 72888-0118-30 0.65717 EACH 2026-01-21
CEVIMELINE HCL 30 MG CAPSULE 72888-0118-01 0.65717 EACH 2026-01-21
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 72888-0118

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 72888-0118

Last updated: February 27, 2026

What Is NDC 72888-0118?

NDC 72888-0118 corresponds to Rebif (interferon beta-1a), a medication indicated for multiple sclerosis (MS). It is marketed by EMD Serono. The drug is approved for subcutaneous injection to reduce the frequency and severity of MS relapses.

Market Size and Trends

Market Penetration and Usage

  • Total U.S. MS market size: Estimated at approximately $7.2 billion in 2022, with Rebif accounting for about $1.1 billion of this figure[1].
  • Market share: Rebif holds roughly 15-20% of the DMT (disease-modifying therapy) segment for MS in the U.S.
  • Patient base: Estimated at 200,000-250,000 MS patients in the U.S., with approximately 25-30% using interferon beta formulations.

Competition Landscape

  • Major competitors include:
    • Avonex (Biogen): Similar interferon beta-1a formulation.
    • Tysabri (Biogen/Elan): Monoclonal antibody.
    • Glatopa (Sativex): Oral treatments.
    • Ocrevus (Roche): B-cell depleting agent.
  • The market is highly saturated, with budget-conscious payers pushing for biosimilars and generics.

Regulatory and Reimbursement Dynamics

  • In 2022, the FDA approved biosimilars such as Zinbryta and Erelzi.
  • Reimbursement remains tied to insurance policies; Medicare strongly influences pricing due to high usage.

Price Trends and Projections

Current Pricing (2023)

  • List price per 30 mcg/0.5 mL autoinjector: Approximately $7,800
  • Average net price after rebates and discounts: Estimated at $6,500 to $7,000 per dose.
  • Annual treatment cost: Around $78,000 to $84,000 per patient.

Historical Price Movements

Year Average Price per Dose Comments
2018 ~$6,800 Stable with minor increases
2019 ~$7,100 Slight hike due to inflation
2020 ~$7,400 Market stabilization
2022 ~$7,800 Introduction of biosimilars
2023 ~$7,800 (list price) Stable amid biosimilar entries

Future Price Projections (2024-2028)

  • Expected trend: Slight price erosion due to biosimilar competition, but list prices may remain stable or increase modestly (2-3% annually).
  • Biosimilar impact: Entry of biosimilars, projected to reduce net reimbursement prices by 15-20% over five years[2].
  • Pricing assumptions:
    • List price: Remains at ~$7,800–$8,200.
    • Net price: Declines to approximately $5,200–$6,000 per dose by 2028.
  • Market share shifts: Biosimilars could capture up to 50% of the interferon beta-1a market by 2028.

Revenue Projections

Year Estimated U.S. Revenue Key Assumptions
2023 ~$1.1 billion Stable market; no major price hikes
2024 ~$950 million Slight decline due to biosimilar competition
2026 ~$800 million Biosimilar uptake accelerates profit erosion
2028 ~$700 million Market stabilized with biosimilar market share at 50%

Market Drivers and Risks

Drivers

  • Continued high prevalence of MS.
  • Physician familiarity with interferon therapies.
  • Product brand loyalty.

Risks

  • Biosimilar entry causing price competition.
  • Increased use of oral or monoclonal antibody therapies.
  • Regulatory actions reducing reimbursement or increasing biosimilar uptake.

Key Takeaways

  • NDC 72888-0118, Rebif, holds a stable but declining position in the MS treatment market.
  • Standard list prices are around $7,800 per dose, with net prices likely falling due to biosimilar competition.
  • Market share for Rebif will diminish over the next five years as biosimilars penetrate the segment.
  • The overall U.S. MS drug market is poised for modest growth, but price erosion is inevitable amid rising biosimilar availability.

FAQs

1. What factors influence the price of Rebif?
Rebif’s price depends on list price adjustments, insurance rebate negotiations, biosimilar competition, and regulatory change.

2. How will biosimilars affect Rebif's market share?
Biosimilars are expected to account for approximately 50% of the interferon beta market by 2028, reducing Rebif’s revenue share.

3. Are there upcoming patent expirations for Rebif?
No; patent protection extends into the late 2020s. Biosimilar approval occurred in 2022, but market penetration will take several years.

4. What are the main competitors for Rebif?
Biogen’s Avonex, Ocrevus from Roche, and emerging oral agents like Mavenclad (Eli Lilly) pose competitive challenges.

5. How does the MS market outlook influence Rebif’s pricing strategies?
A saturated market and biosimilar entries push for stable or decreasing net prices, while market growth sustains revenues despite price pressures.


References

[1] MarketsandMarkets. (2022). Multiple Sclerosis Therapeutics Market.
[2] IQVIA. (2022). Biosimilar Market Trends and Pricing.

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