The Enoxaparin Injection, cataloged under National Stock Number 6505-01-615-1997, is classified within Federal Supply Class 6505 (Drugs and Biologicals) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Amphastar Pharmaceuticals, Inc.. Government technical data includes 6 specifications, cited from the U.S. Government catalog. The record lists 3 manufacturer part numbers for this item, enabling identification through both NSN and commercial part number lookups. 3 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog.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 | 6505-01-615-1997 |
| Primary Part Number | NDC00548-5602-00 |
| Item Name | Enoxaparin Injection |
| FSC / FSG | 6505 / 65 — Drugs and Biologicals |
| Manufacturer | Amphastar Pharmaceuticals, Inc. |
| Status | ACTIVE |
| Administration | INTRAVENOUS OR SUBCUTANEOUS |
| Primary Container Content Quantity | 0.4 MILLILITERS |
| Primary Container Type | SYRINGE |
| Protective Storage Feature | CONTROLLED ROOM TEMPERATURE |
| Raw Material Source | PORCINE INTESTINAL MUCOSA |
| Total Primary Container Quantity | 10 |
| 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 |
|---|---|
| NDC00548-5602-00 PRIMARY | Amphastar Pharmaceuticals, Inc. (USA) |
| NDC00075-0620-40 PRIMARY | Sanofi-Aventis U.s. Llc (USA) |
| NDC00955-1004-10 PRIMARY | Sanofi-Aventis U.s. Llc (USA) |
| Reference | Meaning |
|---|---|
| LOVENOX | 5/1 Secondary reference Sanofi-Aventis U.s. Llc |
| 6505NCM128843 | 5/1 Secondary reference Defense Medical Standardization Board |
| 341611 | 5/1 Secondary reference U.S. Government activity |
NSN 6505-01-615-1997 is a Enoxaparin Injection, manufactured by Amphastar Pharmaceuticals, Inc., classified under FSC 6505, Drugs and Biologicals. Status: active.
NSN 6505-01-615-1997 has 3 manufacturer part numbers on file: NDC00548-5602-00 (Amphastar Pharmaceuticals, Inc.), NDC00075-0620-40 (Sanofi-Aventis U.s. Llc), NDC00955-1004-10 (Sanofi-Aventis U.s. Llc).
Key specifications for NDC00548-5602-00: Administration: INTRAVENOUS OR SUBCUTANEOUS; Primary Container Content Quantity: 0.4 MILLILITERS; Primary Container Type: SYRINGE; Special Features: 40 MG ACTIVE INGREDIENT PER 0.4 ML WATER FOR INJECTION; 40 MG SIZE, GRADUATED, PREFILLED, ONE TIME USE SINGLE DOSE SYRINGE WITH A 27 G X 0.5 IN NEEDLE; PACKAGE OF 10; PRESERVATIVE FREE; FOR SUBCUTANEOUS AND INTRAVENOUS USE; INDICATED FOR THE PROPHYLAXIS OF DEEP VEIN THROMBOSIS (DVT); STORE AT USP CONTROLLED ROOM TEMPERATURE; EXCURSIONS PERMITTED TO 15-30 DEG C (59-86 DEG F); AVAILABLE WITH A SYSTEM THAT SHIELDS THE NEEDLE AFTER INJECTION. STORE AT 25 (77 F); EXCURSIONS PERMITTED TO 15 TO 30 DEG C (59 TO 86 DEG F) (SEE USP CONTROLLED ROOM TEMPERATURE) G. 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.