FDA.reportPublic FDA data

NDC 73377-077-03 - Toltrazuril

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
73377-077
Requested NDC
73377-077-03
Package NDCs from labels
73377-077-01, 73377-077-02, 73377-077-03
Manufacturer
AX Pharmaceutical Corp
Effective date
2026-01-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Toltrazuril - AX Pharmaceutical CorpAX Pharmaceutical Corp2026-01-16BULK INGREDIENT - ANIMAL DRUG

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-077TOLTRAZURIL POWDER [AX PHARMACEUTICAL CORP]23 package rows20210223_2c0d170c-c3c0-4a14-9d63-bbca915a4cba.zip

Reported adverse events (FAERS/openFDA)#

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