FDA.reportPublic FDA data

NDC 54771-5224-3 - Excede Sterile

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
54771-5224
Requested NDC
54771-5224-3
Package NDCs from labels
54771-5224-3, 54771-5224-1, 54771-5224-4, 54771-5224-2
Manufacturer
Zoetis Inc.
Effective date
2026-08-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
EXCEDE ® (Ceftiofur Crystalline Free Acid) Sterile SuspensionZoetis Inc.2026-08-25PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54771-5224-1ExcedeSterile1 in 1 CARTONINJECTION, SUSPENSION111
54771-5224-2ExcedeSterile1 in 1 CARTONINJECTION, SUSPENSION111
54771-5224-3ExcedeSterile100 mL in 1 BOTTLEINJECTION, SUSPENSION10011
54771-5224-4ExcedeSterile250 mL in 1 BOTTLEINJECTION, SUSPENSION25011

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54771-5224EXCEDE STERILE (CEFTIOFUR) INJECTION, SUSPENSION [ZOETIS INC.]84 package rows20240608_9922e056-dcb0-46fd-bb56-9863bb0a189e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ceftiofurACTIVE INGREDIENT83JL932I1CEXCEDE STERILE (CEFTIOFUR) INJECTION, SUSPENSION [ZOETIS INC.]1
ceftiofurACTIVE MOIETY83JL932I1CEXCEDE STERILE (CEFTIOFUR) INJECTION, SUSPENSION [ZOETIS INC.]1

Reported adverse events (FAERS/openFDA)#

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