FDA.reportPublic FDA data

NDC 54771-6045 - Anthelcide EQ

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
54771-6045
Package NDCs from labels
54771-6045-2, 54771-6045-1
Manufacturer
Zoetis Inc.
Effective date
2026-01-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ANTHELCIDE ® EQ (oxibendazole) pasteZoetis Inc.2026-01-27OTC ANIMAL DRUG LABEL
ANTHELCIDE ® EQ (oxibendazole)Zoetis Inc. | Zoetis LLC | UQUIFA Mexico, S.A. DE C.V.2014-03-06OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54771-6045-2Anthelcide EQ24 g in 1 SYRINGEPASTE243

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54771-6045ANTHELCIDE EQ (OXIBENDAZOLE) PASTE [ZOETIS INC.]21 package rows20200402_c3564269-28e8-4852-9a7c-cc6937cce9ae.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
oxibendazoleACTIVE INGREDIENT022N12KJ0XANTHELCIDE EQ (OXIBENDAZOLE) PASTE [ZOETIS INC.]1
oxibendazoleACTIVE MOIETY022N12KJ0XANTHELCIDE EQ (OXIBENDAZOLE) PASTE [ZOETIS INC.]1

Reported adverse events (FAERS/openFDA)#

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