NDC 54771-1504-4 - RIMADYL

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
54771-1504
Requested NDC
54771-1504-4
Package NDCs from labels
54771-1504-1, 54771-1504-2, 54771-1504-3, 54771-1504-4
Manufacturer
Zoetis Inc.
Effective date
2024-02-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
RIMADYL ® (carprofen)Zoetis Inc.2024-02-06PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54771-1504-1RIMADYL7 in 1 BOTTLE, PLASTICTABLET, CHEWABLE73
54771-1504-2RIMADYL30 in 1 BOTTLE, PLASTICTABLET, CHEWABLE303
54771-1504-3RIMADYL60 in 1 BOTTLE, PLASTICTABLET, CHEWABLE603
54771-1504-4RIMADYL180 in 1 BOTTLE, PLASTICTABLET, CHEWABLE1803

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54771-1504RIMADYL (CARPROFEN) TABLET, CHEWABLE [ZOETIS INC.]34 package rows20240207_dbc05493-d1cc-4c00-be6b-d1e3352273fd.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
carprofenACTIVE INGREDIENTFFL0D546HORIMADYL (CARPROFEN) TABLET, CHEWABLE [ZOETIS INC.]1
carprofenACTIVE MOIETYFFL0D546HORIMADYL (CARPROFEN) TABLET, CHEWABLE [ZOETIS INC.]1

Reported adverse events (FAERS/openFDA)#

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