NDC 13985-524-04 - Prevail

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
13985-524
Requested NDC
13985-524-04
Package NDCs from labels
13985-524-02, 13985-524-04
Manufacturer
VetOne/MWI | Bimeda Inc., Division of Cross Vetpharm Group | Bimeda-MTC Division of Cross Vetpharm Group
Effective date
2024-04-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PrevailVetOne/MWI | Bimeda Inc., Division of Cross Vetpharm Group | Bimeda-MTC Division of Cross Vetpharm Group2024-04-01PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13985-524PREVAIL (FLUNIXIN MEGLUMINE) SOLUTION [VETONE/MWI]13Unmatched20240402_934aac52-55d3-48a1-a84c-894d540a7a0e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FLUNIXIN MEGLUMINEACTIVE INGREDIENT8Y3JK0JW3UPREVAIL (FLUNIXIN MEGLUMINE) SOLUTION [VETONE/MWI]2
FLUNIXINACTIVE MOIETY356IB1O400PREVAIL (FLUNIXIN MEGLUMINE) SOLUTION [VETONE/MWI]2

Reported adverse events (FAERS/openFDA)#

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