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NDC61958-2901-02 — REMDESIVIR,INJECTION

✓ Government record, cited
— · COMPONENT
PRODUCT OVERVIEW

NDC61958-2901-02: REMDESIVIR,INJECTION.

The REMDESIVIR,INJECTION is a the manufacturer industrial component. Key specifications include administration: INTRAVENOUS, primary_container_type: VIAL, secondary_container_type: BOX, primary_container_content_quantity: 100.0 MILLIGRAMS, part_name_assigned_by_controlling_agency: REMDESIVIR INJECTION, STERILE POWDER, 100MG VIAL. This part is cataloged in the U.S.

Government catalog under NSN 6505-01-695-6725, indicating validated use in U.S. government and defense logistics supply chains. Available through authorized enterprise resellers and TPM (Third Party Maintenance) channels.

Verify compatibility with your specific system configuration before ordering.

WHERE IT FITS
NDC61958-2901-02
NSN: 6505-01-695-6725
FSC: 6505 — Drugs and Biologicals
CAGE: 0SFJ8 — GILEAD SCIENCES INC (USA)
SPECIFICATIONS
administrationINTRAVENOUS
primary_container_typeVIAL
secondary_container_typeBOX
primary_container_content_quantity100.0 MILLIGRAMS
part_name_assigned_by_controlling_agencyREMDESIVIR INJECTION, STERILE POWDER, 100MG VIAL
NSN6505-01-695-6725
COMPONENT DIAGRAM
COMPONENT MAIN IC EDGE CONNECTOR No detailed specs available REMDESIVIR,INJECTION TITLE COMPONENT PN NDC61958-2901-02 MFR REMDESIVIR,INJECTION
KEY FEATURES
•
ADMINISTRATION: INTRAVENOUS
•
PRIMARY CONTAINER CONTENT QUANTITY: 100.0 MILLIGRAMS
•
SECONDARY CONTAINER TYPE: BOX
•
PRIMARY CONTAINER TYPE: VIAL
TECHNICAL CHARACTERISTICS
ADMINISTRATIONINTRAVENOUS
PRIMARY CONTAINER CONTENT QUANTITY100.0 MILLIGRAMS
SECONDARY CONTAINER TYPEBOX
PRIMARY CONTAINER TYPEVIAL
SPECIAL FEATURESINDICATED FOR ADULTS AND PEDIATRIC PATIENTS (12 YEARS OF AGE AND OLDER AND WEIGHING AT LEAST 40 KG); FOR THE TREATMENT OF CORONAVIRUS DISEASE 2019 (COVID-19) REQUIRING HOSPITALIZATION; THE LYOPHILIZED FORMULATION NEEDS TO BE RECONSTITUTED AND THEN DILUTED INTO NORMAL SALINE IV INFUSION FLUIDS PRIOR TO USE; THE LYOPHILIZED POWDER CAN BE STORED BELOW 86F (30C) PRIOR TO USE. AFTER RECONSTITUTION, USE VIALS IMMEDIATELY TO PREPARE DILUTED SOLUTION; THE DILUTED SOLUTION IN THE INFUSION BAGS CAN BE STORED UP TO 24 HOURS AT ROOM TEMPERATURE 20 C TO 25 C (68 F TO 77 F) PRIOR TO ADMINISTRATION OR 48 HOURS AT REFRIGERATED TEMPERATURE 2 C TO 8 C (36 F TO 46 F); INTENDED FOR INTRAVENOUS ADMINISTRATION; SUPPLIED AS A SINGLE-DOSE VIAL CONTAINING A STERILE, PRESERVATIVE FREE WHITE TO OFF-WHITE TO YELLOW LYOPHILIZED POWDER; 100 MG; DISCARD UNUSED PORTION. KG
PART NAME ASSIGNED BY CONTROLLING AGENCYREMDESIVIR INJECTION, STERILE POWDER, 100MG VIAL
OTHER ITEMS IN FSC 6505 — Drugs and Biologicals
Items in the same Federal Supply class. No interchangeability or substitution relationship is implied.
6505-00-000-0073 6505-00-000-0110 6505-00-000-0134 6505-00-000-0135 6505-00-001-3344 6505-00-001-3345 6505-00-001-3346 6505-00-001-3347
SUBSTITUTES & CROSS-REFERENCES 2
1597230Reference document
Same NSN cross-reference
Reference document — Secondary reference
6505NCM217172Reference document
Same NSN cross-reference
Reference document — Secondary reference
LIFECYCLE
NSN statusActive· U.S. Government catalog
Shelf-life managedNo demilitarization required
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FREQUENTLY ASKED QUESTIONS
What is NDC61958-2901-02?
NDC61958-2901-02 is a REMDESIVIR,INJECTION.
What parts can replace NDC61958-2901-02?
There are 2 known substitutes for NDC61958-2901-02: 1597230, 6505NCM217172. Substitute compatibility should be verified for your specific system.
What is the NSN for NDC61958-2901-02?
NDC61958-2901-02 is cataloged in the U.S. Government catalog under NSN 6505-01-695-6725. This indicates validated use in U.S. government and defense supply chains.
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