FDA.reportPublic FDA data

Toltrazuril

Manufacturer
AX Pharmaceutical Corp
Effective date
2026-01-16
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
3
Source
full-release
Hydrated at
2026-06-01 02:52:20

Label at a glance#

ProductToltrazuril
Active ingredientTOLTRAZURIL
Label structure1 sections

Label contents#

Full prescribing information#

Toltrazuril

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-077-01Toltrazuril0.5 kg in 1 JARPOWDER0.53
73377-077-02Toltrazuril25 kg in 1 DRUMPOWDER253
73377-077-03Toltrazuril5 kg in 1 BAGPOWDER53

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73377-07773377-077-01, 73377-077-02, 73377-077-03

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
TOLTRAZURILQVZ3IAR3JSACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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