FDA.reportPublic FDA data

NDC 51311-009-60 - MOVODYL

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
51311-009
Requested NDC
51311-009-60
Package NDCs from labels
51311-009-60, 51311-009-80
Manufacturer
Virbac AH, Inc.
Effective date
2024-07-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
MOVODYL TM Chewable Tablets (carprofen)Virbac AH, Inc.2024-07-25PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51311-009-60MOVODYL60 in 1 BOTTLE, PLASTICTABLET, CHEWABLE605
51311-009-80MOVODYL180 in 1 BOTTLE, PLASTICTABLET, CHEWABLE1805

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51311-009MOVODYL (CARPROFEN) TABLET, CHEWABLE [VIRBAC AH, INC.]52 package rows20240726_64b63612-56c9-4e53-8991-9ef2fad36826.zip

Reported adverse events (FAERS/openFDA)#

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