FDA.reportPublic FDA data

NDC 54771-8181-2 - Cerenia

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
54771-8181
Requested NDC
54771-8181-2
Package NDCs from labels
54771-8181-2, 54771-8181-1, 54771-8181-3
Manufacturer
Zoetis Inc.
Effective date
2022-08-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cerenia ® (maropitant citrate) TabletsZoetis Inc.2022-08-31PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54771-8181-1Cerenia60 in 1 BOTTLETABLET609
54771-8181-2Cerenia4 in 1 BLISTER PACKTABLET49
54771-8181-3Cerenia10 in 1 CARTONTABLET109
54771-8181-3Cerenia4 in 1 BLISTER PACKTABLET49

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54771-8181CERENIA (MAROPITANT CITRATE) TABLET [ZOETIS INC.]94 package rows20221213_3bc065ce-09d6-4131-a5a0-dca3909e0bc8.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
maropitant citrateACTIVE INGREDIENTLXN6S3999XCERENIA (MAROPITANT CITRATE) TABLET [ZOETIS INC.]1
MAROPITANTACTIVE MOIETY4XE2T9H4DHCERENIA (MAROPITANT CITRATE) TABLET [ZOETIS INC.]1

Reported adverse events (FAERS/openFDA)#

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