FDA.reportPublic FDA data

NDC 71052-026 - Ceftiofur

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
71052-026
Package NDCs from labels
71052-026-25, 71052-026-01
Manufacturer
DARMERICA, LLC
Effective date
2026-01-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ceftiofur - DARMERICA, LLCDARMERICA, LLC2026-01-09BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-026-01Ceftiofur1 kg in 1 PACKAGEPOWDER14
71052-026-25Ceftiofur2.5 kg in 1 PACKAGEPOWDER2.54

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-026CEFTIOFUR POWDER [DARMERICA, LLC]32 package rows20241222_d10fd9cb-a6d3-4df4-a1eb-1906fa143a06.zip

Reported adverse events (FAERS/openFDA)#

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