The Alteplase for Injection, cataloged under National Stock Number 6505-01-717-0237, is classified within Federal Supply Class 6505 (Drugs and Biologicals) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Genentech Usa, Inc. The record lists 1 manufacturer part number 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through both NSN and commercial part number lookups. 3 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog.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: EA.
| Parameter | Value |
|---|---|
| NSN | 6505-01-717-0237 |
| Primary Part Number | NDC50242-0041-64 |
| Item Name | Alteplase for Injection |
| FSC / FSG | 6505 / 65 — Drugs and Biologicals |
| Manufacturer | Genentech Usa, Inc |
| 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 | EA |
| Part Number | Manufacturer |
|---|---|
| NDC50242-0041-64 PRIMARY | Genentech Usa, Inc (USA) |
| Reference | Meaning |
|---|---|
| CATHFLO ACTIVASE | 5/1 Secondary reference Genentech Usa, Inc |
| 1660518 | 5/1 Secondary reference U.S. Government activity |
| 6505NCM239512 | 5/1 Secondary reference Defense Medical Standardization Board |
NSN 6505-01-717-0237 is a Alteplase for Injection, manufactured by Genentech Usa, Inc, classified under FSC 6505, Drugs and Biologicals. Status: active.
NSN 6505-01-717-0237 has 1 manufacturer part number on file: NDC50242-0041-64 (Genentech Usa, Inc).
Key specifications for NDC50242-0041-64: Special Features: A TISSUE PLASMINOGEN ACTIVATOR (T PA) IS A STERILE, WHITE TO PALE YELLOW, LYOPHILIZED POWDER FOR INTRACATHETER, INSTILLATION FOR RESTORATION OF FUNCTION TO CENTRAL VENOUS ACCESS DEVICES FOLLOWING RECONSTITUTION WITH STERILE WATER FOR INJECTION; SUPPLIED AS A STERILE, LYOPHILIZED POWDER IN 2 MG VIALS; STORE AT REFRIGERATED TEMPERATURE (2 8 C/36 46 F).; Part Name Assigned by Controlling Agency: CATHFLO ACTIVASE 2MG. 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.