FDA.reportPublic FDA data

NDC 86136-023-50 - FluoroFlox

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
86136-023
Requested NDC
86136-023-50
Package NDCs from labels
86136-023-50
Manufacturer
MWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITED
Effective date
2026-02-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
FluoroFlox - MWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITEDMWI/Vetone | FELIX PHARMACEUTICALS PRIVATE LIMITED2026-02-18Prescription Animal Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86136-023-50FluoroFlox50 in 1 BOTTLETABLET, CHEWABLE504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86136-023FLUOROFLOX (MARBOFLOXACIN) TABLET, CHEWABLE [MWI/VETONE]31 package rows20241121_359115b7-cdbc-4642-8b4d-c537699758b1.zip

Reported adverse events (FAERS/openFDA)#

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