The Capreomycin Sulfate, cataloged under National Stock Number 6505-01-654-7966, is classified within Federal Supply Class 6505 (Drugs and Biologicals) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Akorn, Inc.. Government technical data includes 8 specifications, cited from the U.S. Government catalog. The record lists 2 manufacturer part numbers 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through both NSN and commercial part number lookups. 1 additional reference document (drawings, advisory and superseded references) is recorded in the U.S. Government catalog.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.
| Parameter | Value |
|---|---|
| NSN | 6505-01-654-7966 |
| Primary Part Number | NDC17478-080-50 |
| Item Name | Capreomycin Sulfate |
| FSC / FSG | 6505 / 65 — Drugs and Biologicals |
| Manufacturer | Akorn, Inc. |
| Status | ACTIVE |
| Administration | INTRAVENOUS AND INTRAMUSCULAR |
| Primary Container Content Quantity | 10.0 MILLILITERS AFTER RECONSTITUTION |
| Medical Designation and Grade | UNITED STATES PHARMACOPEIA |
| Features Provided | STERILE |
| Primary Container Type | VIAL |
| Physical Form | FREEZE-DRIED POWDER |
| Protective Storage Feature | CONTROLLED ROOM TEMPERATURE |
| Active Medicament Medicinal Strength | 1.0 GRAMS CAPREOMYCIN EQUIVALENT G |
| Acquisition Status | ACTIVE |
| DEMIL Code | DEMIL A — No Demilitarization Required |
| Hazard | Possible hazard — SDS may be required (DLA HMIC P) |
| Criticality Code | X |
| Part Number | Manufacturer |
|---|---|
| CAP0105G | Aah Pharmaceuticals Ltd (GBR) |
| NDC17478-080-50 PRIMARY | Akorn, Inc. (USA) |
| Reference | Meaning |
|---|---|
| CAPASTAT | 5/1 Secondary reference Akorn, Inc. |
NSN 6505-01-654-7966 is a Capreomycin Sulfate, manufactured by Akorn, Inc., classified under FSC 6505, Drugs and Biologicals. Status: active.
NSN 6505-01-654-7966 has 2 manufacturer part numbers on file: CAP0105G (Aah Pharmaceuticals Ltd), NDC17478-080-50 (Akorn, Inc.).
Key specifications for NDC17478-080-50: Administration: INTRAVENOUS AND INTRAMUSCULAR; Primary Container Content Quantity: 10.0 MILLILITERS AFTER RECONSTITUTION; Medical Designation and Grade: UNITED STATES PHARMACOPEIA; Features Provided: STERILE. 8 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.