FDA.reportPublic FDA data

NDC 13985-978-10 - Enrosite Flavored

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
13985-978
Requested NDC
13985-978-10
Package NDCs from labels
13985-978-10, 13985-978-05
Manufacturer
MWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITED
Effective date
2026-02-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Enrosite Flavored - MWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITEDMWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITED2026-02-24Prescription Animal Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13985-978-05EnrositeFlavored500 in 1 BOTTLETABLET5006
13985-978-10EnrositeFlavored100 in 1 BOTTLETABLET1006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13985-978ENROSITE FLAVORED (ENROFLOXACIN) TABLET [MWI/VETONE]42 package rows20230620_3b07f056-9281-42dc-9b6d-ac3e267df594.zip

Reported adverse events (FAERS/openFDA)#

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