The Tenecteplase for Injection Kit, cataloged under National Stock Number 6505-01-691-6941, is classified within Federal Supply Class 6505 (Drugs and Biologicals) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Genentech 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through both NSN and commercial part number lookups. 3 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog.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 | 6505-01-691-6941 |
| Primary Part Number | NDC50242-0120-47 |
| Item Name | Tenecteplase for Injection Kit |
| FSC / FSG | 6505 / 65 — Drugs and Biologicals |
| Manufacturer | Genentech 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 |
|---|---|
| NDC50242-0120-47 PRIMARY | Genentech Inc (USA) |
| Reference | Meaning |
|---|---|
| 1584763 | 5/1 Secondary reference U.S. Government activity |
| 6505NCM206571 | 5/1 Secondary reference Defense Medical Standardization Board |
| TNKASE | 5/1 Secondary reference Genentech Inc |
NSN 6505-01-691-6941 is a Tenecteplase for Injection Kit, manufactured by Genentech Inc, classified under FSC 6505, Drugs and Biologicals. Status: active.
NSN 6505-01-691-6941 has 1 manufacturer part number on file: NDC50242-0120-47 (Genentech Inc).
Key specifications for NDC50242-0120-47: Special Features: INDICATED FOR USE IN THE REDUCTION OF MORTALITY ASSOCIATED WITH ACUTE MYOCARDIAL INFARCTION (AMI); TISSUE PLASMINOGEN ACTIVATOR (TPA) PRODUCED BY RECOMBINANT DNA TECHNOLOGY USING AN ESTABLISHED MAMMALIAN CELL LINE (CHINESE HAMSTER OVARY CELLS); STORE LYOPHILIZED TNKASE AT CONTROLLED ROOM TEMPERATURE NOT TO EXCEED 30 C (86 F) OR UNDER REFRIGERATION 2 TO 8 C (36 TO 46 F); DO NOT USE BEYOND THE EXPIRATION DATE STAMPED ON THE VIAL; FOR USE IN MYOCARDIAL INFARCTION; FOR INTRAVENOUS ADMINISTRATION ONLY; EACH KIT CONTAINS ONE 50 MG VIAIAL OF TNKASE, ONE 10 ML VIAL OF PRESERVATIVE-FREE STERILE WATER FOR INJECTION, USP, ONE BD 10 ML SYRINGE WITH TWINPAK DUAL CANNULA DEVICE, AND PACKAGE INSERT CONTAINING FULL PRESCRIBING INFORMATION; VIAL CONTENTS: THE PRESERVATIVE-FREE SINGLE-USE VIAL OF TNKASE CONTAINS 52.5 MG TENECTEPLASE, 0.55 G L-ARGININE, 0.17 G PHOSPHORIC ACID, AND 4.3 MG POLYSORBATE 20, UNDER PARTIAL VACUUM. NO U.S. STANDARD OF POTENCY; 36 MONTHS SHELF LIFE. G; Part Name Assigned by Controlling Agency: TENECTEPLASE INTRAVENOUS KIT, 50MG. 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.