The Moxidectin Injectio, cataloged under National Stock Number 6509-01-732-6942, is classified within Federal Supply Class 6509 (Drugs and Biologicals, Veterinary Use) of the Medical, Dental, and Veterinary Equipment group. The manufacturer of record is Zoetis Inc.. 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through both NSN and commercial part number lookups. 3 additional reference documents (drawings, advisory and superseded references) are recorded in the U.S. Government catalog.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: BX.
| Parameter | Value |
|---|---|
| NSN | 6509-01-732-6942 |
| Primary Part Number | 10004112 |
| Item Name | Moxidectin Injectio |
| FSC / FSG | 6509 / 65 — Drugs and Biologicals, Veterinary Use |
| Manufacturer | Zoetis Inc. |
| Status | ACTIVE |
| Acquisition Status | ACTIVE |
| DEMIL Code | DEMIL A — No Demilitarization Required |
| Hazard | No hazard code in the DLA record (HMIC N) |
| Criticality Code | X |
| Unit of Issue | BX |
| Part Number | Manufacturer |
|---|---|
| 10004112 PRIMARY | Zoetis Inc. (USA) |
| 058854 | Covetrus North America, Llc (USA) |
| 07-893-0220 | Patterson Veterinary Supply, Inc. Div Patterson Veterinary Supply (USA) |
| Reference | Meaning |
|---|---|
| 1696830 | 5/1 Secondary reference U.S. Government activity |
| NDC54771-3671-01 | 3/1 Design control — primary reference Zoetis Inc. |
| 6509NCM251853 | 5/1 Secondary reference Defense Medical Standardization Board |
NSN 6509-01-732-6942 is a Moxidectin Injectio, manufactured by Zoetis Inc., classified under FSC 6509, Drugs and Biologicals, Veterinary Use. Status: active.
NSN 6509-01-732-6942 has 3 manufacturer part numbers on file: 10004112 (Zoetis Inc.), 058854 (Covetrus North America, Llc), 07-893-0220 (Patterson Veterinary Supply, Inc. Div Patterson Veterinary Supply).
Key specifications for 10004112: Special Features: INDICATED FOR USE IN DOGS 6 MONTHS OF AGE AND OLDER FOR THE PREVENTION OF HEARTWORM DISEASE CAUSED BY DIROFILARIA IMMITIS FOR 6 MONTHS, ALSO INDICATED FOR TREATMENT OF EXISTING LARVAL AND ADULT HOOKWORM (ANCYLOSTOMA CANINUM AND UNCINARIA STENOCEPHALA) INFECTIONS; CONTRAINDICATED IN ANIMALS PREVIOUSLY FOUND TO BE HYPERSENSITIVE TO THIS DRUG OR PROHEART 12; BOX INCLUDES 5 VIALS 10 PERCENT (598MG/VIAL) MOXIDECTIN MICROSPERES (10MG/ML AFTER CONSTITUTION), 5- 17ML VIALS OF STERILE VEHICLE, 5 VENT NEEDLES; STORAGE: UNCONSTITUTED AT OR BELOW 25DEG C (77DEG F)/ DO NOT EXPOSE TO LIGHT FOR EXTENDED PERIODS OF TIME, AFTER CONSTITUTION PRODUCT IS STABLE FOR 8 WEEKS STORED UNDER REFRIGERATION AT 2-8DEG C (36-46DEG F); FOR SUBCUTANEOUS USE ONLY. DEGC; Part Name Assigned by Controlling Agency: PROHEART 6, MOXIDECTIN KIT, FOR EXTENDED-RELEASE, VIAL, 20ML, 5S.. 0 specifications are documented in the U.S. Government catalog.
No hazard code in the DLA record (HMIC N). 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.