FDA.reportPublic FDA data

NDC 54771-1691-1 - Palladia

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
54771-1691
Requested NDC
54771-1691-1
Package NDCs from labels
54771-1691-1
Manufacturer
Zoetis Inc.
Effective date
2023-09-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Palladia ® (toceranib phosphate) TabletsZoetis Inc.2023-09-11PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54771-1691-1Palladia30 in 1 BOTTLE, PLASTICTABLET304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54771-1691PALLADIA (TOCERANIB PHOSPHATE) TABLET [ZOETIS INC.]41 package rows20220721_ae09ae83-0812-4ddc-92e3-730f7a1ae449.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
toceranib phosphateACTIVE INGREDIENT24F9PF7J3RPALLADIA (TOCERANIB PHOSPHATE) TABLET [ZOETIS INC.]1
toceranibACTIVE MOIETY59L7Y0530CPALLADIA (TOCERANIB PHOSPHATE) TABLET [ZOETIS INC.]1

Reported adverse events (FAERS/openFDA)#

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