The Cefamandole Nafate for Injection, cataloged under National Stock Number 6505-01-308-9436, is classified within Federal Supply Class 6505 (Drugs and Biologicals) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Eli Lilly and Company. Government technical data includes 6 specifications, cited from the U.S. Government catalog. The record lists 1 manufacturer part number for this item, enabling identification through both NSN and commercial part number lookups. 1 additional reference document (drawings, advisory and superseded references) is recorded in the U.S. Government catalog. Current acquisition status: Active. Unit of issue: PG.
| Parameter | Value |
|---|---|
| NSN | 6505-01-308-9436 |
| Primary Part Number | NDC00002-7268-25 |
| Item Name | Cefamandole Nafate for Injection |
| FSC / FSG | 6505 / 65 — Drugs and Biologicals |
| Manufacturer | Eli Lilly and Company |
| Status | ACTIVE |
| Primary Container Content Quantity | 1.000 GRAMS OF ACTIVE INGREDIENT G |
| Medical Designation and Grade | UNITED STATES PHARMACOPEIA |
| Primary Container Type | VIAL, SINGLE DOSE |
| Physical Form | POWDER |
| Active Medicament Medicinal Strength | 1.000 GRAMS CEFAMANDOLE EQUIVALENT G |
| Total Primary Container Quantity | 25 |
| 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 |
|---|---|
| NDC00002-7268-25 PRIMARY | Eli Lilly and Company (USA) |
| Reference | Meaning |
|---|---|
| MANDOL ADD-VANTAGE | 5/1 Secondary reference Eli Lilly and Company |
NSN 6505-01-308-9436 is a Cefamandole Nafate for Injection, manufactured by Eli Lilly and Company, classified under FSC 6505, Drugs and Biologicals. Status: active.
NSN 6505-01-308-9436 has 1 manufacturer part number on file: NDC00002-7268-25 (Eli Lilly and Company).
Key specifications for NDC00002-7268-25: Primary Container Content Quantity: 1.000 GRAMS OF ACTIVE INGREDIENT G; Medical Designation and Grade: UNITED STATES PHARMACOPEIA; Primary Container Type: VIAL, SINGLE DOSE; Physical Form: POWDER. 6 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.