FDA.reportPublic FDA data

NDC 54771-3362 - Naxcel

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
54771-3362
Package NDCs from labels
54771-3362-1, 54771-3362-2
Manufacturer
Zoetis Inc.
Effective date
2023-07-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Naxcel ®Zoetis Inc.2023-07-25PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54771-3362-1Naxcel12 in 1 CARTONPOWDER126
54771-3362-1Naxcel1 g in 1 VIALPOWDER16
54771-3362-2Naxcel4 g in 1 VIALPOWDER46
54771-3362-2Naxcel6 in 1 CARTONPOWDER66

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54771-3362NAXCEL (CEFTIOFUR SODIUM) POWDER [ZOETIS INC.]64 package rows20230726_b6fed070-b398-4348-9927-9891f78c7c31.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ceftiofur sodiumACTIVE INGREDIENTNHI34IS56ENAXCEL (CEFTIOFUR SODIUM) POWDER [ZOETIS INC.]1
ceftiofurACTIVE MOIETY83JL932I1CNAXCEL (CEFTIOFUR SODIUM) POWDER [ZOETIS INC.]1
potassium phosphate, monobasicINACTIVE INGREDIENT4J9FJ0HL51NAXCEL (CEFTIOFUR SODIUM) POWDER [ZOETIS INC.]1
sodium hydroxideINACTIVE INGREDIENT55X04QC32INAXCEL (CEFTIOFUR SODIUM) POWDER [ZOETIS INC.]1

Reported adverse events (FAERS/openFDA)#

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