This Solicitation opportunity from Department Of Defense was posted on April 27, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.
AMPHOTERICIN B LIPO
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Amphotericin B Liposomal for Injection is a sterile, non-pyrogenic, lyophilized product containing 50 mg of amphotericin B per vial, intended solely for intravenous infusion. Each package unit consists of ten single-use vials with a minimum of 21 months of remaining shelf life at the time of receipt by the first government activity, and the total shelf life is 24 months with no extensions permitted. Unopened vials must be stored at temperatures not exceeding 25°C (77°F), and once reconstitution is performed using sterile water for injection, the resulting concentrate may be stored for up to 24 hours at 2°C to 8°C (36°F to 46°F), with no freezing allowed. The pH of the reconstituted suspension must remain between 5 and 6. Each carton includes one pre-packaged, disposable sterile 5-micron filter. All labeling and packaging must comply with Medical Marking Standard No. 1A, superseding MIL-STD-129, and conform to DLA’s Master List of Technical and Quality Requirements. The product is manufactured by Astellas Pharma US, Inc., with NDC number 00469-3051-30, and the unit of issue is one package per unit (PG = 10 EA). The contract mandates delivery FOB destination within 20 days to Fort Bragg, North Carolina, using traceable shipping methods only, excluding parcel post. The item is regulated by the FDA, and all packaging must adhere to commercial standards compliant with ASTM D3951 unless designated hazardous under FED-STD-313, in which case additional requirements apply. All technical, quality, and marking specifications are binding and take precedence over any general commercial standards.
General Info
Agency
NAICS
Place of Performance
5234 EAGLE TALON DR BLDG X3063, FORT BRAGG, NC, 28310, USASet-Aside
Documents
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Full Description
AMPHOTERICIN B LIPOSOMAL FOR INJECTION
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RA001: THIS DOCUMENT INCORPORATES TECHNICAL AND/OR QUALITY REQUIREMENTS
(IDENTIFIED BY AN 'R' OR AN 'I' NUMBER) SET FORTH IN FULL TEXT IN THE
DLA MASTER LIST OF TECHNICAL AND QUALITY REQUIREMENTS FOUND ON THE WEB
AT:
http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx
FOR SIMPLIFIED ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE SOLICITATION ISSUE DATE OR THE AWARD DATE CONTROLS. FOR LARGE ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE RFP ISSUE DATE APPLIES UNLESS A SOLICITATION AMENDMENT INCORPORATES A FOLLOW-ON REVISION, IN WHICH CASE THE AMENDMENT DATE CONTROLS.
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
. RX ONLY, FOR INTRAVENOUS INFUSION ONLY.. STERILE, NON-PYROGENIC
LYOPHILIZED PRODUCT FOR INTRAVENOUS INFUSION.. EACH VIAL CONTAINS 50 MG
OF AMPHOTERICIN B,USP. FOLLOWING RECONSTITUTION WITH STERILE WATER FOR
INJECTION, USP, THE RESULTING PH OF THE SUSPENSION IS BETWEEN 5-6. EACH
CARTON CONTAINS ONE PRE-PACKAGED, DISPOSABLE STERILE 5 MICRON FILTER..
UNIT OF ISSUE IS A PACKAGE CONTAINING 10 SINGLE USE VIALS. TOTAL SHELF
LIFE IS 24 MONTHS.. THERE SHALL BE A MINIMUM OF 21 MONTHS OF REMAINING
SHELF LIFE AT THE TIME OF RECIPT BY THE FIRST GOVERNMENT ACTIVITY..
UNOPENED VIALS OF LYOPHILIZED MATERIAL ARE TO BE STORED AT TEMPERATURES
UP TO 25° C (77° F).. THE RECONSTITUTED PRODUCT CONCENTRATE MAY BE
STORED FOR UP TO 24 HOURS AT 2º-8º C (36º-46º F) FOLLOWING
RECONSTITUTION WITH STERILE WATER FOR INJECTION, USP.. DO NOT FREEZE.
. LABELING AND MARKING MUST IN ACCORDANCE WITH MEDICAL MARKING STANDARD
NO. 1A DATED 4 FEBRUARY 2013. 5/6/2015
1 PG = 10 EA
.
This device or drug is regulated by the FDA. Note to Buyers: The contracting official shall send a referral in EBS to the product specialist for confirmation. Please include bidder name and bidder contact information, manufacturer name, manufacturer part number, and item description.
APPLICABLE TO ALL MEDICAL ACQUISITIONS:
PACKAGING AND PACKING SHALL BE COMMERCIAL AS SPECIFIED IN THE PROCUREMENT DOCUMENT.
EACH COMPLETE UNIT SHALL BE PROPERLY PACKAGED IN A SUITABLE SEALED UNIT CONTAINER CAPABLE OF PROTECTING THE CONTENTS FROM DAMAGE AND/OR BREAKAGE.
UNITS SHALL BE PACKED IN SUITABLE COMMERCIAL EXTERIOR (SHIPPING) CONTAINERS (EXPORT WHEN NECESSARY) WHICH SHALL INSURE ACCEPTANCE AND SAFE DELIVERY BY COMMON OR OTHER CARRIER, AT THE LOWEST RATE, TO POINT OF DELIVERY CALLED FOR IN THE CONTRACT OR ORDER.
MATERIAL MUST BE MARKED IAW MEDICAL MARKING STANDARD NO. 1. THIS SUPERCEDES ALL REFERENCES TO MIL-STD-129.
SPE2DP-26-T-3132
SECTION B
COPIES OF MEDICAL MARKING STANDARD NO. 1
(MMS NO. 1) MAY BE OBTAINED BY CONTACTING DLA
TROOP SUPPORT VIA EMAIL TO fssb@dla.mil. MMS NO. 1 IS ALSO AVAILABLE ONLINE AT: https://www.dla.mil/Logistics-Operations/Packaging/
RD003, COVERED DEFENSE INFORMATION POTENTIALLY APPLIES
RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a shelf life of 24 months (non-extendable) applies to this item.
SHALL BE MARKED IAW THE LATEST EDITION OF
THE MEDICAL MARKING STANDARD NO. 1.
MMS NO. 1 IS AVAILABLE ONLINE AT:
https://www.dla.mil/Logistics-Operations/Packaging/
ASTELLAS PHARMA US, INC. 39832 P/N NDC00469-3051-30
DLA issues this document using the DoD authorized unit of issue, please refer to the following URL to determine the corresponding ANSI X12 unit of issue.
https://view.officeapps.live.com/op/view.aspx?src=https%3A%2F%2Fwww.dla.mil%2FPortals%2F104%2FDocuments% 2FDLMS%2FeApplications%2FLogDataAdmin%2FUnitofIssueandPurchaseUnit.xlsx&wdOrigin=BROWSELINK
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0001 7016505402 0001 PG 1.000
NSN/MATERIAL:6505015396542
DELIVERY (IN DAYS):0020
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
BULK BREAK POINT:
SPE2DP-26-T-3132
SECTION B
PR: 7016505402 PRLI: 0001 CONT’D
W91KBP
0003 SF BN 01 CO A SUSTAINMEN
3D SFG SSA AWCF SSF
5234 EAGLE TALON DR BLDG X3063
FORT BRAGG NC 28310
US
SHIP BY TRACEABLE MEANS. DO NOT USE PARCEL POST.
FREIGHT SHIPPING ADDRESS:
W91KBP
0003 SF BN 01 CO A SUSTAINMEN
3D SFG SSA AWCF SSF
5234 EAGLE TALON DR BLDG X3063
FORT BRAGG NC 28310
US
MARKFOR
W91KBP
0003 SF BN 01 CO A SUSTAINMEN
3D SFG SSA AWCF SSF
5234 EAGLE TALON DR BLDG X3063
FORT BRAGG NC 28310
US
M/F: (TCN) W91KBP61060057
RDD: 120
PROJ: TP 3
SUPP ADD: W9046W SIG: C
FOR GOVERNMENT USE ONLY: (IPD) 12
DIC: A0A DIST: V ADV: 2A FC: Z9
Need Ship Date:00/00/0000 Original Required Delivery Date:04/28/2026
SPE2DP-26-T-3132 NSN/Part Number: 6505-01-539-6542 Quantity: 1 PG Purchase Request: 7016505402QTY: 1 Delivery: 20 days ADO
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