NDC 54771-2718-4 - Dectomax Pour-On

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
54771-2718
Requested NDC
54771-2718-4
Package NDCs from labels
54771-2718-2, 54771-2718-3, 54771-2718-4
Manufacturer
Zoetis Inc.
Effective date
2023-07-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
DECTOMAX® Pour-OnZoetis Inc.2023-07-24OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54771-2718-2DectomaxPour-On1000 mL in 1 BOTTLESOLUTION100010
54771-2718-3DectomaxPour-On2500 mL in 1 JUGSOLUTION250010
54771-2718-4DectomaxPour-On5000 mL in 1 JUGSOLUTION500010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54771-2718DECTOMAX POUR-ON (DORAMECTIN) SOLUTION [ZOETIS INC.]103 package rows20230912_ec6ff537-4773-432d-86db-7ba767769c80.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
doramectinACTIVE INGREDIENTKGD7A54H5PDECTOMAX POUR-ON (DORAMECTIN) SOLUTION [ZOETIS INC.]1
doramectinACTIVE MOIETYKGD7A54H5PDECTOMAX POUR-ON (DORAMECTIN) SOLUTION [ZOETIS INC.]1

Reported adverse events (FAERS/openFDA)#

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