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2K SERVICE ENTERPRISE LLC

UEI: DNCKRVDAJHL3CAGE: 6S9J3

2K SERVICE ENTERPRISE LLC is a federal contractor, registered under UEI DNCKRVDAJHL3 and CAGE code 6S9J3. It has been awarded $205,460 across 10 federal contracts. Primary work spans In-Vitro Diagnostic Substance Manufacturing and Pharmaceutical Preparation Manufacturing. Top awarding agencies include Department Of Veterans Affairs.

Contact Information

Registration and classification details

Address123 Main St, City, ST 12345

Registration

UEI Code

DNCKRVDAJHL3

CAGE Code

6S9J3

Entity Structure

Sole Proprietorship

Established

N/A

Business Classifications

23272X8E8WA2A5LJPIQF

NAICS Codes

518210Computing Infrastructure Providers, Data Processing, Web Hosting, and Related Services

541511Custom Computer Programming Services

541512Computer Systems Design Services

541611Administrative Management and General Management Consulting Services(Primary)

541612Human Resources Consulting Services

+4 more

Federal Contracting Overview

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

AI Capability Profile

2K SERVICE ENTERPRISE LLC specializes in professional, scientific, and technical services under NAICS 541511, delivering tailored IT and systems support solutions to federal and defense clients. Their core capabilities encompass software development, systems integration, and technical consulting ser...

Key Performance Metrics

Awards Count

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Past period of performance

Total Awards

All time

Contracts

Prime · all time

Subcontracts

Sub · all time

Grants

Prime · all time

Subgrants

Sub · all time

Award Analytics & Distribution

Awards by Agency

Department Of Veterans Affairs$205.5K100%

Awards by NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing$138.0K67.2%

325412 - Pharmaceutical Preparation Manufacturing$67.5K32.8%

Awards by Agency Over Time

Awards by Place of Performance

Open opportunities in 2K SERVICE ENTERPRISE LLC's top NAICS codes and agencies

CIPROFLOXACIN TABLETSCiprofloxacin tablets, 500 mg unit dose in packages of 100, are being procured under solicitation SPE2DP-26-T-4316 with the NSN 6505012738650, requiring a total of three units of issue, each representing 100 tablets. The item must comply with all technical and quality standards listed in the DLA Master List of Technical and Quality Requirements, including specific packaging guidelines that mandate commercial packaging consistent with Medical Marking Standard No. 1, which supersedes MIL-STD-129. Each unit must be sealed in a container that protects against damage, and all shipments must be packed in commercial exterior containers suitable for safe delivery via common carrier at the lowest cost to the specified destination. The product has a non-extendable shelf life of 36 months and must bear labels and markings in full compliance with medical marking standards. The supplier, The Harvard Drug Group, L.L.C., must deliver the item FOB destination within 20 days of contract award, with no variance allowed in quantity. Inspection and acceptance occur at the delivery point, and all materials must be prepared in accordance with MIL-STD-2073-1E. The contract includes applicable defense information controls, and government identification must be removed from any non-accepted supplies. The solicitation opened on July 27, 2026, with a response deadline of August 3, 2026, and is being managed by the Department of Defense’s Medical Supply Chain PHARM FSA with direct contact through James Foggie.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

MECLIZINE HYDROCHLORIDMeclizine Hydrochloride Tablets USP, containing 25 milligrams of the active ingredient per tablet, are procured in bottles of 1,000 tablets, with a total shelf life of 24 months and a mandatory minimum of 21 months remaining at the time of receipt by the first government activity. The product must be stored at controlled room temperature between 20°C and 25°C (68°F to 77°F) as per USP standards. Packaging must comply with commercial standards and meet the Medical Marking Standard No. 1, superseding MIL-STD-129, with all containers designed to prevent damage and ensure safe transport via common carrier at the lowest cost to the destination. The item is regulated by the FDA and requires referral to a product specialist for confirmation prior to award. The contract specifies delivery to Fort Bragg, North Carolina, within 20 days, with no variance allowed in quantity. The unit of issue is a bottle (BT), and palletization must follow DLA packaging requirements. The drug is supplied by approved manufacturers including Amneal Pharmaceuticals and Jubilant Cadista, with NDC identifiers provided. The material is not classified as hazardous per Fed-Std-313 and must be commercially packaged in accordance with ASTM D3951, though DLA’s Master List of Technical and Quality Requirements takes precedence. Shipments must be traceable and不得 use parcel post. The solicitation number is SPE2DP-26-T-4296, with a response deadline of August 3, 2026, and the required delivery date is July 28, 2026.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

ACYCLOVIR TABLETSThe contract pertains to the procurement of 3 bottles of 800 mg acyclovir tablets, each bottle containing 100 tablets, under solicitation SPE2DP-26-T-4323, with delivery required within 20 days FOB destination. The product must meet strict packaging standards as defined by Medical Marking Standard No. 1, superseding MIL-STD-129, and must be packed in sealed unit containers that prevent damage, with exterior shipping containers ensuring safe, cost-effective delivery via common carrier. The acyclovir tablets are sourced from approved manufacturers including Golden State, Teva, GSK Zovirax, Carlsbad Tech, and Mylan, each identified by specific NDC codes. The item carries a non-extendable 24-month shelf life as a Type I (Code M) item, and no mercury or mercury-containing compounds may be introduced into the product or packaging, except for specific exceptions such as batteries or instruments meeting NAVSEA specifications. The contract follows DLA’s master list of technical and quality requirements, and units must be marked in accordance with DLA’s medical marking guidelines. Inspection and acceptance occur at the delivery point with zero variance allowed in quantity, and the unit of issue is bottles (BT). The contract is issued under the Department of Defense, with performance located at Fort Bragg, and all documentation must align with DoD authorized unit of issue standards.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

LORATADINE TABLETSLoratadine tablets 10 mg are being procured in bulk quantities of 500 tablets per unit, with a total requirement of three units (BT), each containing 500 tablets, under solicitation SPE2DP-26-T-4315. The product is regulated by the FDA and must comply with strict packaging and marking standards, specifically Medical Marking Standard No. 1, which replaces all references to MIL-STD-129; packaging must be commercial grade, sealed to prevent damage, and suitable for safe transport via common carrier at the lowest cost to the destination point specified in the contract. The item has a non-extendable shelf life of 36 months and must be stored between 20°C and 25°C (68°F to 77°F), protected from excessive moisture. The manufacturer is OHM Laboratories Inc with NDC 51660-0526-05, distributed by AmerisourceBergen Drug Corp, and the NSN is 6505-01-524-9179. Delivery is required within 20 days FOB destination with zero variance allowed on quantity, and inspection and acceptance occur at the delivery point. The contract mandates compliance with DLA’s Master List of Technical and Quality Requirements, and any applicable defense information controls under RD003. All packaging must be labeled in accordance with MMS No. 1, accessible via the DLA website, and the contracting official must submit a referral in EBS to confirm bidder and manufacturer details prior to award.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

MOXIFLOXACIN HYDROCHLOMoxifloxacin Hydrochloride Tablets, 400 mg in 30-count bottles, are procured under solicitation SPE2DP-26-T-4320 with a requirement for three bottles, delivered FOB destination within 20 days. The item is regulated by the FDA and must comply with the Medical Marking Standard No. 1, superseding MIL-STD-129, with all packaging and labeling adhering strictly to its specifications. Each unit must be sealed in commercial packaging capable of preventing damage and shipped in exterior containers suitable for safe transport via common carrier at the lowest rates. The product carries a non-extendable shelf life of 36 months and must be stored at controlled room temperature away from high humidity. The supplier must be identified by NDC number—either Teva Pharmaceuticals USA Inc. NDC 00093-7387-56 or Rising Pharma Holdings Inc. NDC 57237-0156-30—and all documentation must include bidder and manufacturer details for FDA referral via EBS. The unit of issue is bottle, and no variance in quantity is permitted. Packaging must meet MIL-STD-2073-1E standards, and delivery is to Fort Stewart, GA, with inspection and acceptance occurring at destination.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

BUPIVACAINE HYDROCHLORThe contract specifies the procurement of BUPIVACAINE HYDROCHLORIDE INJECTION, USP, 0.25%, in 50 mL vials, with a total quantity of 5 bottles, to be delivered within 20 days to Fort Bragg, North Carolina. The product is regulated by the FDA and must meet strict shelf-life requirements of 24 months with no extensions, and storage must be maintained between 20 °C to 25 °C, with allowable excursions between 15 °C to 30 °C. Packaging and labeling must comply with MIL-STD-129, DLA’s Packaging Requirements for Procurement, and ASTM D3951 for non-hazardous materials, though DLA’s technical and quality requirements take precedence. The item is marked with NDC00409-1587-50 and sourced from PFIZER INC, with unit of issue BT and no variance allowed in quantity. Delivery is FOB destination, with inspection and acceptance occurring at the destination point. The shipment must be sent via traceable means and not parcel post. The contracting entity is the Department of Defense, under the Medical Supply Chain Pharm FSA, with the solicitation number SPE2DP-26-T-4293, and the required delivery date is July 28, 2026. All technical and quality specifications referenced in the DLA Master List are binding and must be adhered to, and the product is subject to covered defense information protocols.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

DIPHENHYDRAMINE HYDThe contract specifies the procurement of 50mg DIPHENHYDRAMINE HYDROCHLORIDE CAPSULES,USP in 100-count bottles, with a total order of 12 bottles (5 units of 1 bottle and 7 units of 1 bottle), delivered FOB destination within 20 days of the required delivery date of July 29, 2026. The item is regulated by the FDA and carries a non-extendable 24-month shelf life under Type I (Code M) requirements. Packaging must comply with DLA’s RP001 standards, MIL-STD-129 labeling, and the DLA Master List of Technical and Quality Requirements, taking precedence over commercial standards like ASTM D3951. The product must be shipped via traceable freight without parcel post, and all packaging must indicate the manufacturer as RICHMOND PHARMACEUTICALS, INC. with NDC54738-0116-01 and be palletized per DLA directives. Delivery is directed to Fort Bragg, North Carolina, under contract SPE2DP-26-T-4313, with no variance allowed in quantity. The contract also requires strict adherence to the federal marking and hazardous material handling protocols, including the incorporation of RD003 for covered defense information and RA001 for technical and quality compliance. All documentation and submissions must reference the DLA eProcurement portal for applicable requirements, and the contracting official must submit an EBS referral to confirm product eligibility.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

LEVONORGESTREL AND ETHThe contract specifies the procurement of LEVONORGESTREL AND ETHINYL ESTRADIOL TABLETS, USP, a hormonal contraceptive medication regulated by the FDA, manufactured by TEVA PHARMACEUTICALS USA, INC. with NDC 00555-9047-58. Each unit consists of six 28-day cycles totaling 168 tablets, formulated in a sequential pattern: six tablets containing 0.050 mg levonorgestrel and 0.030 mg ethinyl estradiol, followed by five tablets with 0.075 mg levonorgestrel and 0.040 mg ethinyl estradiol, then ten tablets with 0.125 mg levonorgestrel and 0.030 mg ethinyl estradiol, concluding with seven inert tablets. The unit of issue is one package containing 168 tablets, and the product must have a minimum of 21 months of remaining shelf life upon receipt by the government, with a total shelf life of 24 months non-extendable. Storage must be maintained at controlled room temperature, between 20° and 25°C (68° to 77°F), per USP guidelines. All packaging and labeling must strictly comply with Medical Marking Standard No. 1A dated February 4, 2013, superseding MIL-STD-129, and must be commercially packaged to ensure protection during transport. Packaging must be sealed in suitable containers to prevent damage and delivered in commercial shipping containers at the lowest feasible freight rate to the designated delivery point at Fort Stewart, Georgia. Delivery is required within 20 days of contract award, with no variance allowed in quantity, and inspection and acceptance occur at the destination. The shipment must be sent by the fastest traceable means, excluding parcel post, and must adhere to all DLA Master List of Technical and Quality Requirements, which take precedence over other standards such as ASTM D3951. The contract is part of a federal solicitation under SPE2DP-26-T-4311, with the purchasing agency being the Department of Defense through the Medical Supply Chain Pharm FSA.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

LABETALOL HYDROCHLORIDLabetalol Hydrochloride Injection USP, 5 mg per mL in 40 mL vials, is being procured under solicitation SPE2DP-26-T-4294 with a required delivery of four vials within twenty days to Fort Stewart, Georgia, FOB destination. Each vial is a single unit of issue and must conform to FDA regulations and the DLA Master List of Technical and Quality Requirements, including specifications outlined under RQ011, RS016, and RS001, which mandate a non-extendable shelf life of twenty-four months and proper medical marking per the latest Medical Marking Standard No. 1. The product is manufactured by Hikma Pharmaceuticals USA Inc. with NDC 00143-9623-01 and must be stored at medical controlled room temperature. The purchase request number is 7017618337, and the NSN is 6505012579990; zero variance is permitted in quantity, and inspection and acceptance occur at the delivery point. Packaging must meet MIL-STD-2073-1E standards, and all government identification must be removed from non-accepted supplies in accordance with RD003. The contracting official is required to submit a referral in EBS to the product specialist with full bidder and manufacturer details prior to award.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

DEXTROSE AND SODIUM CHDextrose and Sodium Chloride Injection USP is a sterile, nonpyrogenic, single-dose intravenous solution containing 5 grams of anhydrous dextrose and 0.45 grams of sodium chloride per 100 mL, packaged in 1-liter bags with one port, and is latex-free but contains DEHP. Each package contains twelve 1-liter containers, and the product must be stored at 20 to 25°C with protection from excessive heat and freezing; it must not be used if the solution is cloudy or seals are compromised. The item is regulated by the FDA, has a non-extendable shelf life of 30 months, and must be marked in accordance with Medical Marking Standard No. 1 and MIL-STD-129. Packaging must comply with DLA’s RP001 requirements and ASTM D3951 if nonhazardous, with all DLA technical requirements taking precedence. The unit of issue is a box (BX), with one box containing twelve 1-liter bags, and delivery is required within ten days FOB destination to the specified address in Baumholder, Germany. The procurement is under solicitation SPE2DP-26-T-4324, with a required delivery date of July 29, 2026, and the National Stock Number is 6505-00-116-1025. The product is identified by NDC 00990-7926-09 and provided by ICU Medical Sales, Inc. Government use documentation and compliance with DLA procurement standards are mandatory, including referral through EBS and adherence to all applicable DLA Master List requirements, with point of contact for inquiries listed as Daniel Porter.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

IVERMECTIN TABLETSIvermectin tablets, 3 mg in unit dose, are procured in packages of 20 tablets per unit, with a total quantity of one package required under solicitation SPE2DP-26-T-4310. The product must comply with strict packaging standards as defined by Medical Marking Standard No. 1, superseding MIL-STD-129, and must be shipped in commercial-grade containers designed to prevent damage and ensure safe delivery at the lowest freight cost to Fort Bragg, North Carolina, 28310. Storage must be maintained below 30°C (86°F), and the item has a non-extendable shelf life of 24 months as a Type I (Code M) item. The tablets are regulated by the FDA and require confirmation by the product specialist via EBS referral, including full manufacturer and part number details. Two manufacturers are identified: Merck Sharp & Dohme Corp. with NDC 00006-0032-20 and Edenbridge Pharmaceuticals, LLC with NDC 42799-0806-01. Delivery is FOB destination within 20 days, with zero tolerance for quantity variance, and inspection and acceptance occur at the point of delivery. All markings, packaging, and documentation must adhere to DLA’s updated technical and quality requirements as referenced in the DLA Master List, and the item is identified by NSN 6505-01-491-9286.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

ALBUTEROL SULFATE INHA

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

SODIUM CHLORIDE INJECTSodium Chloride 0.9% Injection, USP, 500 mL in packs of 24 units is being procured under solicitation SPE2DP-26-T-4212 by the Department of Defense’s Medical Supply Chain PHARM FSA for delivery to Prince Hassan Air Base in Safawi, Jordan. The contract requires 8 packs, with delivery due 20 days after order placement, and products must meet all FDA regulatory standards for pharmaceuticals. Packaging must follow commercial standards as specified in the procurement document, with each unit sealed in a protective container and shipped in commercial exterior containers capable of safe transportation at the lowest rate. Marking must conform to Medical Marking Standard No. 1, which supersedes MIL-STD-129 for all medical items, and packaging must comply with MIL-STD-2073-1E. A strict 24-month non-extendable shelf life applies, and the product must be free from intentional mercury or mercury-containing compounds, except for functional uses such as batteries or sensors as permitted under NAVSEA 5100-003D. The item is subject to the FAR and DFARS clauses covering cybersecurity, information safeguarding, trafficking in persons, employment eligibility, sustainable products, and prohibition of covered telecommunications equipment. Offerors must be registered in SAM.gov, possess a valid UEI and CAGE code, and comply with socioeconomic representations including small business status. All submissions must be made electronically via the DLA Internet Bid Board System by the closing date of July 27, 2026. Inspection and acceptance occur at the destination, and payment must be requested through Wide Area WorkFlow. Contractor personnel must be informed of whistleblower rights, and any cyber incidents involving covered defense information must be reported in accordance with DFARS clause 252.204-7012. The contract prohibits the use of mandatory arbitration agreements, restricts compensation of former DoD officials, and mandates compliance with NIST SP 800-171 for information system safeguarding. The government reserves the right to reject any non-compliant offer, and the product must be manufactured by an approved vendor such as Baxter, B. Braun, or McKesson, with verified product codes and NDC numbers provided.

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

HYDROGEN PEROXIDE TOPI

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

MEDICAL SUPPLY CHAIN PHARM FSA

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about 20 hours ago

DEADLINE

MULTIPLE ELECTROLYT

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

OMEPRAZOLE EXTENDED-RE

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE

FLUCONAZOLE TABLETS

MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

about 20 hours ago

DEADLINE