6505--Ustekinumab Pens/Syringes or Biosimilar
ID: 36E79726R0006Type: Presolicitation
Overview

Buyer

VETERANS AFFAIRS, DEPARTMENT OFVETERANS AFFAIRS, DEPARTMENT OFNAC PHARMACEUTICALS (36E797)HINES, IL, 60141, USA

NAICS

Pharmaceutical Preparation Manufacturing (325412)

PSC

DRUGS AND BIOLOGICALS (6505)
Timeline
    Description

    The Department of Veterans Affairs (VA) is preparing to issue a Request for Proposal (RFP) for the procurement of Ustekinumab Pens/Syringes or Biosimilars, aimed at supplying various federal health entities including the Department of Defense, Bureau of Prisons, Indian Health Service, and Federal Health Care Center. The contract will be awarded for an initial period of one year, with the possibility of four additional one-year option periods, ensuring a consistent supply of these critical pharmaceutical products through the VA and DoD Pharmaceutical Prime Vendor Programs. Offerors must provide drugs with unique National Drug Code (NDC) numbers and ensure that any biosimilar products meet FDA licensing requirements, as outlined in the FDA Purple Book. The solicitation is expected to be released around January 12, 2026, with a tentative closing date of January 27, 2026; interested parties should direct inquiries to Chris Carthron at Christopher.Carthron@va.gov or (708) 786-4980.

    Point(s) of Contact
    Christopher CarthronContract Specialist
    (708) 786-4980
    Christopher.Carthron@va.gov
    Files
    Title
    Posted
    The VA National Acquisition Center plans to issue RFP 36E79726R0006 for an unrestricted procurement of Ustekinumab Pen/Syringes or Biosimilar. This contract will supply the Department of Veterans Affairs, Department of Defense, Bureau of Prisons, Indian Health Service, and Federal Health Care Center. A single contract will be awarded for one year with four optional one-year periods, distributing items via VA and DoD Pharmaceutical Prime Vendor Programs. Offerors must provide drugs with unique NDC numbers and labels. The solicitation is expected around January 12, 2026, closing tentatively on January 27, 2026, with NAICS code 325412. All documents will be available on sam.gov. Biosimilar products must be FDA-licensed and listed in the FDA Purple Book. Offerors must provide both syringe and vial versions for any strength/line item where both are commercially available, at the same price. Estimated annual usage includes 2,917 units of 5MG/ML, 9,608 units of 45MG/0.5ML, and 45,763 units of 90MG/ML. Chris Carthron is the point of contact.
    Lifecycle
    Title
    Type
    Presolicitation
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