OXIBENDAZOLE

Manufacturer
Professional Compounding Centers of America
Effective date
2023-01-12
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
2
Source
full-release
Hydrated at
2026-06-01 02:51:11

Label at a glance#

ProductOXIBENDAZOLE
Active ingredientOXIBENDAZOLE
Label structure1 sections

Label contents#

Full prescribing information#

OXIBENDAZOLE (FOR VETERINARY USE ONLY)FOR PRESCRIPTION COMPOUNDING/RX ONLYPART: 30-5021CAS: 20559-55-1WARNING:HARMFUL BY INHALATION, SKIN CONTACT & IF SWALLOWED. WEAR PROTECTIVE GLOVES & FACE/EYE PROTECTION.Storage: STORE IN TIGHTLY CLOSED CONTAINER. STORE ...

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXIBENDAZOLE (FOR VETERINARY USE ONLY)
FOR PRESCRIPTION COMPOUNDING/RX ONLY
PART: 30-5021
CAS: 20559-55-1
WARNING:
HARMFUL BY INHALATION, SKIN CONTACT & IF SWALLOWED. WEAR PROTECTIVE GLOVES & FACE/EYE PROTECTION.
Storage: STORE IN TIGHTLY CLOSED CONTAINER. STORE AT ROOM TEMPERATURE.image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51927-5201-0OXIBENDAZOLE1 kg in 1 BOTTLEPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51927-5201OXIBENDAZOLE (OXIBENDAZOL) POWDER [PROFESSIONAL COMPOUNDING CENTERS OF AMERICA]21 package rows20241006_59011ebd-e5e1-494b-b59a-1d92b051f195.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51927-520151927-5201-0
52286-0002

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
OXIBENDAZOLE022N12KJ0XACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.