The Vancomycin,injection, cataloged under National Stock Number 6505-01-687-3772, is classified within Federal Supply Class 6505 (Drugs and Biologicals) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Xellia Pharmaceuticals Usa Llc. The record lists 1 manufacturer part number for this item, enabling identification through both NSN and commercial part number lookups. 2 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog. Current acquisition status: Active. Unit of issue: PG.
| Parameter | Value |
|---|---|
| NSN | 6505-01-687-3772 |
| Primary Part Number | NDC70594-0042-03 |
| Item Name | Vancomycin,injection |
| FSC / FSG | 6505 / 65 — Drugs and Biologicals |
| Manufacturer | Xellia Pharmaceuticals Usa Llc |
| Status | ACTIVE |
| Acquisition Status | ACTIVE |
| DEMIL Code | DEMIL A — No Demilitarization Required |
| Hazard | Possible hazard — SDS may be required (DLA HMIC P) |
| Criticality Code | X |
| Unit of Issue | PG |
| Part Number | Manufacturer |
|---|---|
| NDC70594-0042-03 PRIMARY | Xellia Pharmaceuticals Usa Llc (USA) |
| Reference | Meaning |
|---|---|
| 1570861 | 5/1 Secondary reference U.S. Government activity |
| 6505NCM206078 | 5/1 Secondary reference Defense Medical Standardization Board |
NSN 6505-01-687-3772 is a Vancomycin,injection, manufactured by Xellia Pharmaceuticals Usa Llc, classified under FSC 6505, Drugs and Biologicals. Status: active.
NSN 6505-01-687-3772 has 1 manufacturer part number on file: NDC70594-0042-03 (Xellia Pharmaceuticals Usa Llc).
Key specifications for NDC70594-0042-03: Special Features: A GLYCOPEPTIDE ANTIBACTERIAL INDICATED IN ADULT AND PEDIATRIC PATIENTS (1 MONTH AND OLDER); STERILE; SUPPLIED AS A READY TO USE CLEAR, COLORLESS TO LIGHT BROWN SOLUTION IN SINGLE-DOSE FLEXIBLE BAGS CONTAINING 1G VANCOMYCIN IN 200ML OF LIQUID(CONSIST OF WATER AND PEG TOGEHTER WITH THE EXCIPIENTS NADA AND LYSINE); SEALED ALUMINUM OVERPOUCHES BAG; STORE BELOW25C (77F), IN ORIGINAL PACKAGE; PRODUCT SHOULD BE USED WITHIN 28 DAYS OF REMOVAL FROM ALUMINUM OVERPOUCH; PACK OF 12 BAGS. G; Part Name Assigned by Controlling Agency: VANCOMYCIN INJECTION, SOLUTION, 1G/200ML BAG, 12S G. 0 specifications are documented in the U.S. Government catalog.
Possible hazard — SDS may be required (DLA HMIC P). Hazard information on this page is shown exactly as it appears in the DLA record.
U.S. Government catalog: edition PUBLOGDVD v12.0.0 (OCT 2026), edition date 2026-10-01, retrieved 2026-10-16.
U.S. Government catalog: edition PUBLOGDVD v12.0.0 (OCT 2026), edition date 2026-10-01, retrieved 2026-10-18.