FDA.reportPublic FDA data

NDC 54771-2780 - Librela

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
54771-2780
Package NDCs from labels
54771-2780-1, 54771-2780-2
Manufacturer
Zoetis Inc.
Effective date
2025-02-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
bedinvetmab injection - Zoetis Inc.Zoetis Inc.2025-02-21PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54771-2780-1Librela2 in 1 CARTONINJECTION, SOLUTION24
54771-2780-2Librela6 in 1 CARTONINJECTION, SOLUTION64

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54771-2780LIBRELA (BEDINVETMAB INJECTION) INJECTION, SOLUTION [ZOETIS INC.]42 package rows20250223_61c7b4e0-aab6-4cf5-8471-f94be438c758.zip

Reported adverse events (FAERS/openFDA)#

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