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60 DEGREES PHARMACEUTICALS, INC.

UEI: WKN5DNLTVF95CAGE: 71D06

60 DEGREES PHARMACEUTICALS, INC. is a federal contractor, registered under UEI WKN5DNLTVF95 and CAGE code 71D06. It has been awarded $5,785,459 across 4 federal contracts. Primary work spans Pharmaceutical Preparation Manufacturing. Top awarding agencies include Department Of Defense.

Contact Information

Registration and classification details

Registration

UEI Code

WKN5DNLTVF95

CAGE Code

71D06

Entity Structure

Corporate Entity (Not Tax Exempt)

Established

N/A

Business Classifications

2XMF

NAICS Codes

325412Pharmaceutical Preparation Manufacturing(Primary)

Federal Contracting Overview

Award totals, agency breakdown, NAICS distribution, and geographic footprint.

AI Capability Profile

60 Degrees Pharmaceuticals, Inc. specializes in the commercial-scale manufacturing, packaging, and validation of pharmaceutical preparations, with a demonstrated focus on complex antimalarial therapeutics such as tafenoquine (ARAKODA). The company possesses deep technical expertise in GMP-compliant ...

60 Degrees Pharmaceuticals, Inc. specializes in the commercial-scale manufacturing, packaging, and validation of pharmaceutical preparations, with a demonstrated focus on complex antimalarial therapeutics such as tafenoquine (ARAKODA). The company possesses deep technical expertise in GMP-compliant production workflows, sterile and non-sterile packaging validation, and end-to-end pharmaceutical supply chain support for government-critical medications. Their capability extends to brand-name drug commercialization, including regulatory-aligned labeling, batch documentation, and quality assurance systems tailored to defense and veteran health requirements. What sets them apart is their precision in executing high-integrity pharmaceutical operations under stringent federal oversight, ensuring product stability, traceability, and compliance with FDA and DoD standards. The contractor has delivered critical pharmaceutical services to the Department of Defense and the Department of Veterans Affairs, primarily supporting the procurement and distribution of specialized therapeutics for military personnel and veteran populations. Their work for DoD centers on the commercial-scale packaging and validation of branded antimalarial agents, while their VA engagement involves sustained supply chain support under Federal Supply Schedule contracts for hematological and pharmaceutical products. These relationships reflect a pattern of trusted, repeat engagement for mission-critical drug logistics and readiness support. Operating under NAICS 325412, the company is positioned within the pharmaceutical preparation manufacturing sector, focusing on finished dosage forms rather than active pharmaceutical ingredient synthesis. Their vertical specialization lies in niche, high-stakes therapeutics used in expeditionary and chronic care settings, particularly those requiring stringent cold-chain or stability controls. As a small business structured as a 2L entity based in Washington, D.C., 60 Degrees Pharmaceuticals operates without federal certifications but maintains a strategic presence in the federal pharmaceutical supply market, leveraging proximity to key policy and procurement hubs to support national health security initiatives.

Key Performance Metrics

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Award Analytics & Distribution

Awards by Agency
Department Of Defense$5.8M100%
Awards by NAICS
325412 - Pharmaceutical Preparation Manufacturing$5.8M100%
Awards by Agency Over Time
Export
Awards by Place of Performance

Open opportunities in 60 DEGREES PHARMACEUTICALS, INC.'s top NAICS codes and agencies

NAICS: 325412
New
DIBBS
Veterinary Pharmaceutical Tablet SupplierThe contract requires the manufacture and supply of Maropitant Citrate 160mg veterinary tablets packaged in blister packs containing four tablets per sheet, fully compliant with FDA and Defense Logistics Agency specifications. The product must meet all regulatory and quality standards for veterinary use, with strict adherence to packaging, labeling, and stability requirements to ensure efficacy and safety during storage and transport. The supplier is expected to deliver consistent, high-quality output in accordance with pharmaceutical manufacturing best practices, and all materials must be traceable and documented to support federal procurement compliance. This subcontract is issued under the Medical Supply Chain Pharm FSA, a division of the Department of Defense, with performance required at the APO ZIP code 09227-0000. The solicitation was posted on August 5, 2026, and responses are due by August 11, 2026, indicating a tight turnaround for proposals. The NAICS code 325412 identifies this as a pharmaceutical and biological product manufacturing contract, emphasizing the technical and regulatory expertise necessary for participation. While no set-aside details are provided, the contract is open to qualified subcontractors capable of meeting DoD’s stringent pharmaceutical supply chain requirements, with all deliverables aligned to ensure uninterrupted availability of critical veterinary medications for military and associated personnel.
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NAICS: 325412
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OATMEAL, COLLOIDAL CONC
Solicitation # SPE2DP-26-T-4504
The contract is for Oatmeal, Colloidal Concentrate, a medical supply regulated by the FDA, sourced under the Johnson & Johnson/NDC 81370-0364-00 specification. Each unit is packaged as 8 packets per PG unit, with a total requirement of 3 PG, equating to 24 individual packets. The item carries a non-extendable shelf life of 36 months and must comply with Medical Marking Standard No. 1, replacing all references to MIL-STD-129. Packaging must adhere to MIL-STD-2073-1E, ensuring sealed unit containers protect contents from damage during transport and are packed in commercially suitable exterior containers for safe, cost-effective delivery to the destination point. All markings and labeling must meet DLA medical standards, and copies of the marking guide are available via DLA Troop Support. The contract is issued under solicitation SPE2DP-26-T-4504 with a response deadline of August 11, 2026, and a delivery requirement of 20 days after award, FOB destination. The NSN is 6505-01-442-2051, and quantity variance is strictly zero percent with no tolerance for over or under delivery. Inspection and acceptance occur at the delivery point. The purchase request number is 7017749529, and pricing is set at a unit price of $3.00 per PG. The contracting official must submit a referral in EBS to confirm product compliance, including manufacturer and bidder details. The item falls under NAICS code 325412 and is managed by the Department of Defense’s Medical Supply Chain PHARM FSA office. The delivery location is Fort Campbell, and all requirements are subject to DLA’s master list of technical and quality specifications as referenced by RP001 and RA001.
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NAICS: 325412
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WATER FOR IRRIGATIO
Solicitation # SPE2DP-26-T-4512
Water for Irrigation, Sterile, USP, is a 1000 mL sterile, distilled, and nonpyrogenic solution supplied in semi-rigid plastic containers with screw caps, intended exclusively for irrigation, washing, rinsing, and dilution purposes and not for injection by usual parenteral routes. Each package contains twelve units and is identified by NSN 6505-01-075-0679 and NDC 00338-0004-04, manufactured by Baxter Healthcare Corporation. The product must be stored at controlled room temperature between 20°C and 25°C (68°F to 77°F), protected from freezing and excessive heat, with a non-extendable shelf life of 36 months. Packaging and labeling must strictly adhere to the latest Medical Marking Standard No. 1 and MIL-STD-129, with commercial packaging in compliance with ASTM D3951 unless otherwise specified by DLA’s Master List of Technical and Quality Requirements, which take precedence. All shipments are to be delivered FOB destination within five days, with zero variance allowed in quantity, and are subject to inspection and acceptance at the delivery point. The item is regulated by the FDA, and contractor submissions require referral through EBS for confirmation. Delivery is directed to multiple U.S. Navy vessels across FPO addresses, with specific shipment instructions prohibiting parcel post and requiring traceable transport methods. Palletization and packaging follow DLA’s RP001 requirements, and each order line item is tied to unique contract line item numbers, purchase requests, and delivery schedules ranging from March through August 2026.
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NAICS: 325412
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MOXIFLOXACIN HYDROCHLO
Solicitation # SPE2DP-26-T-4509
Moxifloxacin Hydrochloride Tablets, 400 mg in 30-tablet bottles, are being procured under solicitation SPE2DP-26-T-4509 with a total quantity of 8 bottles, each containing 30 tablets, for delivery within 20 days FOB destination. The item is regulated by the FDA and must comply with the Medical Marking Standard No. 1 dated February 4, 2013, which supersedes all references to MIL-STD-129. Packaging must meet commercial standards as specified in the procurement document, with each unit sealed in a container that protects against damage or breakage and packed in suitable exterior shipping containers to ensure safe delivery at the lowest carrier rate. The product has a non-extendable shelf life of 36 months and must be stored at controlled room temperature, avoiding high humidity. Accepted manufacturers include TEVA PHARMACEUTICALS USA, INC. and RISING PHARMA HOLDINGS, INC., with designated NDC numbers. The contract requires strict adherence to DLA’s Master List of Technical and Quality Requirements, and any covered defense information must be marked in accordance with the latest edition of Medical Marking Standard No. 1. Inspection and acceptance occur at the destination with zero variance permitted in quantity. A referral must be sent via EBS to the product specialist confirming bidder, manufacturer, and product details prior to award.
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NAICS: 325412
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WATER FOR INJECTION, ST
Solicitation # SPE2DP-26-T-4510
Water for Injection, Sterile, USP, is procured in 20ml vials with flip-top closures, packaged in units of 25 vials per package, with a non-extendable shelf life of 24 months. The product must be stored at controlled room temperature between 20–25°C (68–77°F) and marked in accordance with the latest edition of the Medical Marking Standard No. 1. Technical and quality requirements are governed by the DLA Master List of Technical and Quality Requirements, with compliance determined by the revision in effect on the solicitation or award date, depending on acquisition size. The item is regulated by the FDA and requires a referral through EBS to confirm bidder and manufacturer details, including NDC numbers for Hospira Worldwide LLC (NDC 00409-4887-20) and Fresenius Kabi, LLC (NDC 63323-0185-20). The NSN is 6505005825079, with a single package quantity of one unit. Delivery is required within 20 days to Fort Campbell, Kentucky, FOB destination, with no variance allowed in quantity. Inspection and acceptance occur at the delivery point. Packaging must comply with MIL-STD-2073-1E, and government identification must be removed from non-accepted supplies. The solicitation is issued under SPE2DP-26-T-4510, with a response deadline of August 11, 2026, and is classified under NAICS code 325412 by the Department of Defense’s Medical Supply Chain PHARM FSA.
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NAICS: 325412
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LEVONORGESTREL AND ETH
Solicitation # SPE2DP-26-T-4515
The contract specifies the procurement of LEVONORGESTREL AND ETHINYL ESTRADIOL TABLETS, USP, a hormonal contraceptive product regulated by the FDA, supplied by TEVA PHARMACEUTICALS USA, INC. Each package contains 168 tablets organized into six cycles of 28 tablets each, with a controlled sequence of active and inert tablets: six tablets with 50 mcg levonorgestrel and 30 mcg ethinyl estradiol, followed by five tablets with 75 mcg levonorgestrel and 40 mcg ethinyl estradiol, ten tablets with 125 mcg levonorgestrel and 30 mcg ethinyl estradiol, and seven inert tablets. The unit of issue is one package (PG) equaling 168 tablets, with a total order of two packages. The product must have a minimum of 21 months of remaining shelf life at the time of receipt by the first government activity, with a full 24-month shelf life from manufacture. Storage must be maintained at controlled room temperature between 20°C and 25°C (68°F to 77°F). Packaging and labeling must comply strictly with Medical Marking Standard No. 1A dated February 4, 2013, replacing all references to MIL-STD-129, and all units must be sealed in commercial containers that protect against damage and ensure safe, cost-effective delivery to Fort Campbell, TN, with delivery required within 20 days. The product is subject to federal acquisition regulations and requires pre-award confirmation through the EBS referral system, including manufacturer and product identification. The NSN is 6505012240176, the solicitation number is SPE2DP-26-T-4515, and the contract is awarded under a no-variance quantity agreement with FOB destination terms.
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NAICS: 325412
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ENROFLOXACIN INJECT
Solicitation # SPE2DP-26-T-4496
Enrofloxacin Injection, a veterinary antibiotic solution for dogs, is supplied at a concentration of 2.27% with a dosage of 2.5 mg per kilogram in a 20 mL volume, intended for intramuscular use in managing bacterial pathogens. The product is regulated by the FDA and requires strict adherence to shelf-life requirements, with a non-extendable shelf life of 24 months classified as a Type I (Code M) item. Storage must be maintained at or below 25 degrees Celsius with excursions permitted up to 40 degrees Celsius, and the product must be protected from direct sunlight and freezing. Packaging and marking must conform to the latest edition of the Medical Marking Standard No. 1, superseding all references to MIL-STD-129, and all units must be sealed in commercial containers designed to prevent damage and ensure safe transport. The item is procured under contract SPE2DP-26-T-4496 with a single unit of issue, delivered FOB destination within 81 days, with zero variance tolerance. Delivery is directed to the U.S. Medical Material Center in Kaiserslautern, Germany, with the required delivery date set for August 5, 2026. Supplier information includes Patterson Veterinary Supply, Inc. and Covetrus North America, LLC with designated part numbers, and all technical and quality requirements are governed by the DLA Master List of Technical and Quality Requirements. The contracting official must submit a referral via EBS for FDA-regulated product confirmation prior to award, including manufacturer and bidder details.
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NAICS: 325412
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NEOMYCIN AND POLYMYXIN
Solicitation # SPE2DP-26-T-4500
The contract covers the procurement of Neomycin and Polymyxin B Sulfates and Gramicidin, a regulated pharmaceutical product with NDC number 24208-0790-62, supplied by Bausch & Lomb Pharmaceuticals Division under the Veteran’s Health Joint Venture program. The item is classified as a TYPE I (CODE Q) with a strict non-extendable shelf life of 36 months, and all packaging must comply with Medical Marking Standard No. 1, superseding MIL-STD-129. Each unit must be sealed in a protective container and shipped in commercial exterior packaging suitable for safe transport by common carrier at the lowest cost to the delivery point, with all markings adhering to DLA’s medical marking standards. The product is subject to FDA regulation, requiring contracting officials to verify its status via EBS referral prior to award. The delivery is FOB destination, with required shipment within five days of award, and no quantity variance is permitted. The contract includes the NSN 6505-01-143-4643 and references the DLA Master List of Technical and Quality Requirements for applicable specifications, with the solicitation number SPE2DP-26-T-4500 and response deadline set for August 11, 2026. The item is procured under the authorized unit of issue BT (10 mL), with a total quantity of 3 units, and performance is to occur at Fort Lewis, WA. The contract is governed under federal acquisition protocols, and supplier submissions must include detailed information on the bidder, manufacturer, part number, and product description. All packaging and labeling must meet DLA’s technical and quality standards as defined in their official documentation.
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NAICS: 325412
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BENZOCAINE ORAL TOPICA
Solicitation # SPE2DP-26-T-4499
The contract is for the procurement of Benzocaine Oral Topical Gel, 20%, in 1 oz (28g) quantities, identified by NSN 6505-01-064-5769 and NDC 00283-0871-31, under solicitation SPE2DP-26-T-4499. Delivery is required within 20 days after award, with FOB destination terms, and inspection and acceptance will occur at the delivery point. The item has a non-extendable shelf life of 36 months, and all packaging must comply with commercial standards as specified in the procurement document, including sealed unit containers and commercial exterior shipping containers suitable for safe transport at the lowest cost. Packaging and marking must adhere to Medical Marking Standard No. 1, which supersedes MIL-STD-129, and preservation must follow MIL-STD-2073-1E. The product must be marked with appropriate barcoding and labeling as defined by MMS No. 1, available through DLA Troop Support or online. The contract is subject to a zero percent quantity variance and requires electronic invoicing through Wide Area WorkFlow (WAWF). The contract incorporates numerous FAR and DFARS clauses mandating compliance with cybersecurity requirements including NIST SP 800-171, safeguarding of covered defense information, and cyber incident reporting, along with transportation rules requiring U.S.-flag vessels for ocean shipments unless a waiver is granted at least 45 days in advance. Contractors must comply with hazardous material labeling per OSHA standards, immediately report any safety concerns, and ensure all personnel are informed of whistleblower protections. Affirmative representations regarding small business status, socioeconomic certifications including WOSB, SDVOSB, and HUBZone, and Unique Entity ID (UEI) are required. The solicitation is issued using an automated simplified acquisition process, and while the type of contract is not yet specified, the absence of trade-off evaluation factors and reliance on price preferences for small business set-asides suggest a Lowest Price Technically Acceptable (LPTA) award approach. All submissions must be made electronically via the DIBBS portal by the deadline of August 11, 2026, and the contracting office is the Medical Supply Chain Pharm FSA under the Defense Logistics Agency.
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NAICS: 325412
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CHARCOAL, ACTIVATED, SUS
Solicitation # SPE2DP-26-T-4503
Activated charcoal in suspension form, specified as 50 grams per 240 milliliter bottle, is being procured under solicitation SPE2DP-26-T-4503 with a total quantity of six bottles, each unit containing 240 mL. The contract requires full compliance with DLA packaging and marking standards, including adherence to Medical Marking Standard No. 1 which supersedes MIL-STD-129, and all units must be sealed in suitable containers that protect against damage and ensure safe transport at the lowest carrier rate to Fort Bragg, NC 28310. Each bottle must include mandatory labeling with NSN, manufacturer, CAGE code, date of manufacture, expiration or retest date, contract number, and lot number, and no more than five months may have passed from manufacture to government delivery. The product has a 36-month shelf life and must be stored at controlled room temperature between 20°C and 25°C as defined by USP standards. The procurement falls under NAICS code 325412, is managed by the Department of Defense’s Medical Supply Chain Pharm FSA, and requires delivery within 20 days of award. Bidders must clearly state the source and part number being offered, and all technical and quality requirements are governed by the DLA Master List of Technical and Quality Requirements, with the applicable revision determined by the solicitation issue date.
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NAICS: 325412
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SODIUM CHLORIDE INJECT
Solicitation # SPE2DP-26-T-4516
Sodium Chloride Injection 0.9% in 500 mL units, supplied in cases of 24 each, is procured under solicitation SPE2DP-26-T-4516 with a delivery deadline of 20 days FOB destination and no quantity variance permitted. The item is regulated by the FDA and must comply with all applicable medical marking standards, specifically Medical Marking Standard No. 1, which replaces MIL-STD-129. Packaging must meet commercial standards with each unit sealed in a protective container and shipped in durable exterior containers suitable for safe transport via common carrier at the lowest cost. The product has a non-extendable shelf life of 24 months and must not contain intentional mercury or mercury compounds, except for limited exceptions such as functional components in batteries or instruments compliant with NAVSEA 5100-003D. All supplies must be marked with the correct NSN 6505013306268 and adhere to DLA packaging requirements, with government identification removed from non-accepted items. Only approved manufacturers including Baxter Healthcare Corp, B. Braun Medical Inc, McKesson Medical-Surgical, Cardinal Health, ICU Medical Sales, and Tribalco LLC are listed as acceptable sources. The acquisition falls under NAICS code 325412, is a federal procurement, and requires referral to the product specialist via EBS for confirmation prior to award. Contract performance is governed by the DLA Master List of Technical and Quality Requirements, with the revision effective on the solicitation issue date controlling unless amended.
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NAICS: 325412
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TRAZODONE TABLETS
Solicitation # SPE2DP-26-T-4520
The contract specifies the procurement of Trazodone Hydrochloride Tablets in 100 mg strength, packaged in bottles of 100 tablets, with a required shelf life of 24 months from the date of manufacture. At least 21 months must remain on the shelf at the time of delivery to the government, meaning no product can be delivered with less than 21 months of usable life remaining. All labeling and packaging must strictly comply with Medical Marking Standard No. 1A dated February 4, 2013, superseding all references to MIL-STD-129. The product is regulated by the FDA, and the contracting official must submit a referral through EBS to the product specialist prior to award, including bidder and manufacturer details such as name, part number, and item description. Packaging must be commercial-grade, sealed appropriately to prevent damage, and suitable for safe transport via common carrier at the lowest cost to the designated delivery point. The material must be marked and labeled in full accordance with the Medical Marking Standard, and if deemed non-hazardous per FED-STD-313, it must be packed in compliance with ASTM D3951, though DLA’s Master List of Technical and Quality Requirements takes precedence over any conflicting commercial standards. Palletization must follow DLA Packaging Requirements for Procurement, and shipment must be sent by the fastest traceable means, explicitly excluding parcel post. The delivery destination is Fort Bragg, North Carolina, with a required delivery window of 20 days from award and a firm required delivery date of August 7, 2026. The quantity ordered is three bottles, with no tolerance for variance in quantity. The NSN is 6505-01-137-0032, and the unit of issue is "BOTTLE." Approved manufacturers include Mead Johnson & Company, LLC, Teva Pharmaceuticals USA, Inc., and Apotex Corp., each with their respective NDC numbers. The contract identifies the procurement under solicitation number SPE2DP-26-T-4520, issued by the Department of Defense’s Medical Supply Chain Pharmaceutical FSA, with Alec Deichman listed as the primary point of contact. The contract includes specific federal and defense logistics identifiers, freight shipping details, and government-only tracking codes, reinforcing the item’s inclusion under controlled defense acquisition regulations. All packaging, labeling, and fulfillment must adhere to these exacting standards to
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NAICS: 325412
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ALBUTEROL SULFATE INHA
Solicitation # SPE2DP-26-T-4517
Albuterol Sulfate Inhalation Aerosol with HFA is a prescription-only medication delivered as a metered-dose inhaler, with each actuation providing 108 micrograms of albuterol sulfate, equivalent to 90 micrograms of albuterol base, from a 8.5-gram canister containing 200 inhalations. The product must be stored at room temperature between 59°F and 77°F, protected from extreme heat or cold, and must never be punctured, exposed to flames, or thrown into fires due to risk of bursting above 120°F. It is subject to a non-extendable 24-month shelf life as a Type I (Code M) item. Labeling must include the National Stock Number, manufacturer details, manufacturing and expiration dates, contract number, and lot number. The item is regulated by the FDA and requires pre-award referral for confirmation via EBS with full bidder and manufacturer information. Packaging must comply with Commercial standards and Medical Marking Standard No. 1, replacing all references to MIL-STD-129, with each unit sealed in a protective container and shipped in exterior packaging suitable for safe transport at the lowest cost to the delivery point. Safety Data Sheets in compliance with OSHA’s revised Hazard Communication Standard are required pre-award, along with HCS-compliant labeling adhering to 29 C.F.R. 1910.1200 and the Globally Harmonized System. Suppliers must train employees on these requirements. The contract, issued under SPE2DP-26-T-4517, calls for 4 units with delivery due within 20 days FOB destination, zero variance permitted, and inspection and acceptance occurring at destination. The NSN is 6505-01-543-6562, and the unit of issue is each. Multiple manufacturers including Perrigo Direct Inc and Teva Pharmaceuticals USA, Inc. are eligible, with specific NDC numbers referenced. All documentation must align with DLA’s Master List of Technical and Quality Requirements, and covered defense information may apply.
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NAICS: 325412
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TEST STRIPS AND COLOR
Solicitation # SPE2DS-26-T-311U
The contract specifies the procurement of test strips and color charts for the analysis of multiple urine parameters including bilirubin, blood, glucose, ketone, leukocytes, nitrite, pH, protein, specific gravity, and urobilinogen. Each unit of issue consists of one bottle containing 100 test strips, and the item is identified by NSN 6550-01-221-5400 with a single unit requested under purchase request 7017746719. The strips must meet stringent quality and technical requirements as defined in the DLA Master List of Technical and Quality Requirements, and packaging must comply with the Medical Marking Standard No. 1, superseding MIL-STD-129. All units must be sealed in commercial packaging capable of protecting contents from damage and shipped in suitable exterior containers to ensure safe delivery at the lowest freight rate to the designated FPO delivery point with ZIP 09588-2304. The item is classified as a Type I (Code K) shelf-life item with a mandatory 18-month non-extendable shelf life, requiring no more than two months to have elapsed from the date of manufacture to the date of government delivery. Labels must clearly indicate the date of manufacture, expiration or retest date, and the contract number or lot number in accordance with the latest revision of MMS1C. The solicitation, issued under SPE2DS-26-T-311U, was posted on August 5, 2026, with responses due by August 11, 2026, and the delivery requirement is within 20 days after award. The contracting agency is the Department of Defense through the Medical Supply Chain MD Surg FSF, with primary point of contact Mary-Kathryn Donahue.
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NAICS: 325412
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POVIDONE-IODINE CLEANS
Solicitation # SPE2DP-26-T-4384
POVIDONE-IODINE CLEANSING SOLUTION, USP 7.5% active ingredient, for external use only, is being procured under solicitation SPE2DP-26-T-4384 in 1-gallon bottles identified by the unit of issue BT, with a total order of 10 BTs split between two CLINs. Each bottle must have a minimum shelf life of 31 months remaining at the time of delivery to the government activity, with a full 36-month total shelf life and storage requirements between 15°C and 30°C (59°F to 86°F), with 25°C (77°F) as the ideal. The product is regulated by the FDA and subject to strict packaging, marking, and safety standards. Packaging must comply with the Medical Marking Standard No. 1, superseding MIL-STD-129, and all units must be sealed in protective containers with commercial exterior shipping containers to ensure safe transit at the lowest carrier rate. Palletization must follow DLA Packaging Requirements RP001. If classified as hazardous under FED-STD-313, packaging must meet TQ Requirement IP025; otherwise, commercial packaging consistent with ASTM D3951 applies, though DLA’s Technical and Quality Requirements always supersede ASTM standards. Marking and labeling must adhere to OSHA’s Hazard Communication Standard 29 C.F.R. 1910.1200, requiring current Safety Data Sheets and compliant HazCom labels to be submitted for approval prior to award. Employee training on these requirements is mandatory. Delivery is FOB destination to USS HARPERS FERRY LSD 49 at FPO AP 96665, with inspection and acceptance occurring at the destination. The product cannot be shipped via parcel post and must be delivered by traceable means. The solicitation requires electronic response via DIBBS by August 10, 2026, with an original required delivery date of August 3, 2026. The contract incorporates multiple FAR and DFARS clauses including equal opportunity, trafficking in persons, employment eligibility verification, sustainable products, hazardous material identification, and NIST SP 800-171 assessment requirements. Offerors must provide UEI and CAGE codes, certify size status and socioeconomic categories if applicable, and disclose any provision of covered defense telecommunications equipment. Pricing is not specified and will be
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