The Botulism Antitoxin, cataloged under National Stock Number 6505-01-504-5760, is classified within Federal Supply Class 6505 (Drugs and Biologicals) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Department of the Army U S Army Medical Material Agency Mcmr-Mmo-Sa. Government technical data includes 1 specification, 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through both NSN and commercial part number lookups. 1 additional reference document (drawings, advisory and superseded references) is recorded in the U.S. Government catalog.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: VI.
| Parameter | Value |
|---|---|
| NSN | 6505-01-504-5760 |
| Primary Part Number | IND 7451 |
| Item Name | Botulism Antitoxin |
| FSC / FSG | 6505 / 65 — Drugs and Biologicals |
| Manufacturer | Department of the Army U S Army Medical Material Agency Mcmr-Mmo-Sa |
| Status | ACTIVE |
| American Hospital Formulary Service Classification Number | 800400 |
| 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 | VI |
| Part Number | Manufacturer |
|---|---|
| IND 7451 PRIMARY | Department of the Army U S Army Medical Material Agency Mcmr-Mmo-Sa (USA) |
| Reference | Meaning |
|---|---|
| 03-0147 | 5/1 Secondary reference U.S. Government activity |
NSN 6505-01-504-5760 is a Botulism Antitoxin, manufactured by Department of the Army U S Army Medical Material Agency Mcmr-Mmo-Sa, classified under FSC 6505, Drugs and Biologicals. Status: active.
NSN 6505-01-504-5760 has 1 manufacturer part number on file: IND 7451 (Department of the Army U S Army Medical Material Agency Mcmr-Mmo-Sa).
Key specifications for IND 7451: Special Features: BOTULISM EQUINE HEPTAVALENT ANTITOXIN,TYPES A,B,C,D,E,F,AND G(DESPECIATED, FAB 2); LYOPHILIZED POWDER, 23ML VIAL; FOR CONTINGENCY/INVESTIGATIONAL USE ONLY; SINGLE VIAL FOR INTRAVENOUS INJECTION ONLY; PRE-TREATMENT SKIN TESTING IS REQUIRED; Part Name Assigned by Controlling Agency: BOTULISM ANTITOXIN A B C D E F G LYOPHILIZED POWDER 23ML VIAL; American Hospital Formulary Service Classification Number: 800400. 1 specification is 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.