FDA.reportPublic FDA data

NDC 71052-007-01 - Diclazuril

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
71052-007
Requested NDC
71052-007-01
Package NDCs from labels
71052-007-20, 71052-007-50, 71052-007-01, 71052-007-02
Manufacturer
DARMERICA, LLC
Effective date
2026-09-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Diclazuril - DARMERICA, LLCDARMERICA, LLC2026-09-03BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-007-01Diclazuril10 kg in 1 PACKAGEPOWDER105
71052-007-20Diclazuril1 kg in 1 PACKAGEPOWDER15
71052-007-50Diclazuril5 kg in 1 PACKAGEPOWDER55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-007DICLAZURIL POWDER [DARMERICA, LLC]53 package rows20241222_2b9834f7-1dd7-452e-bc07-1ffe91cdea0e.zip

Reported adverse events (FAERS/openFDA)#

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