NDC39822-1055-05: AMPHOTERICIN B FOR INJECTION.
The AMPHOTERICIN B FOR INJECTION is a the manufacturer industrial component. Key specifications include physical_form: FREEZE-DRIED POWDER, administration: INTRAVENOUS INFUSION, primary_container_type: VIAL, supplementary_features: D-DAY ITEM FOR DOD, medical_designation_and_grade: UNITED STATES PHARMACOPEIA, primary_container_content_quantity: 50.000 MILLIGRAMS OF ACTIVE INGREDIENT. This part is cataloged in the U.S.
Government catalog under NSN 6505-01-084-9453, 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.
| physical_form | FREEZE-DRIED POWDER |
| administration | INTRAVENOUS INFUSION |
| primary_container_type | VIAL |
| supplementary_features | D-DAY ITEM FOR DOD |
| medical_designation_and_grade | UNITED STATES PHARMACOPEIA |
| primary_container_content_quantity | 50.000 MILLIGRAMS OF ACTIVE INGREDIENT |
| active_medicament_medicinal_strength | 50.000 MILLIGRAMS AMPHOTERICIN B ACTIVE INGREDIENT |
| part_name_assigned_by_controlling_agency | AMPHOTERICIN B FOR INJECTION USP 50MG BT |
| NSN | 6505-01-084-9453 |
| ADMINISTRATION | INTRAVENOUS INFUSION |
| PRIMARY CONTAINER CONTENT QUANTITY | 50.000 MILLIGRAMS OF ACTIVE INGREDIENT |
| SUPPLEMENTARY FEATURES | D-DAY ITEM FOR DOD |
| MEDICAL DESIGNATION AND GRADE | UNITED STATES PHARMACOPEIA |
| PRIMARY CONTAINER TYPE | VIAL |
| PHYSICAL FORM | FREEZE-DRIED POWDER |
| SPECIAL FEATURES | AMPHOTERICIN B INJECTION USP 50MG PER VIAL - PRIOR TO RECONSTITUTION AMPHOTERICIN B FOR INJECTION USP SHOULD BE STORED UNDER REFRIGERATION, 2 TO 8 C (36 TO 46 F), PROTECTED AGAINST EXPOSURE TO LIGHT. THE CONCENTRATE (5 MG AMPHOTERICIN B PER ML AFTER RECONSTITUTION WITH 10 ML STERILE WATER FOR INJECTION USP) MAY BE STORED IN THE DARK, AT ROOM TEMPERATURE FOR 24 HOURS, OR AT REFRIGERATOR TEMPERATURES FOR ONE WEEK WITH MINIMAL LOSS OF POTENCY AND CLARITY. |
| PART NAME ASSIGNED BY CONTROLLING AGENCY | AMPHOTERICIN B FOR INJECTION USP 50MG BT |
| ACTIVE MEDICAMENT MEDICINAL STRENGTH | 50.000 MILLIGRAMS AMPHOTERICIN B ACTIVE INGREDIENT |