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| NSN | FSC | NIIN | CLS | Hazmat | DEMIL | Cancelled NSN |
|---|---|---|---|---|---|---|
| 6505-01-018-2729 Item PartTypeName: DOXORUBICIN HYDROCHLORIDE FOR IN | 6505 | 010182729 | M | Y | ||
| CIIC | HCC | ESD | PMIC | Criticality | ENAC | |
| U | A | |||||
| Part Number | ISC | RNVC | RNCC | HCC | MSDS | SADC |
| NDC55390-0233-01 | 2 | 2 | 3 |
| MRC | Criteria | Characteristic |
|---|---|---|
| AGXW | PHYSICAL FORM | FREEZE-DRIED POWDER |
| AJCN | PROTECTIVE STORAGE FEATURE | ANTINEOPLASTIC DRUG |
| AKJA | ACTIVE MEDICAMENT MEDICINAL STRENGTH | 1.00 MILLIGRAMS DOXORUBICIN HYDROCHLORIDE ACTIVE INGREDIENT PER ML |
| CQCT | PRIMARY CONTAINER TYPE | VIAL |
| CRLK | PRIMARY CONTAINER CONTENT QUANTITY | 50.000 MILLIGRAMS |
| CXCY | PART NAME ASSIGNED BY CONTROLLING AGENCY | DOXORUBICIN HYDROCHLORIDE FOR INJECTION USP 50MG VIAL |
| FEAT | SPECIAL FEATURES | W/5.000 MG LACTOSE,USP IN EA ML; NOTE: D |
| MDES | MEDICAL DESIGNATION AND GRADE | UNITED STATES PHARMACOPEIA |
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