NDC 13985-707 - 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
13985-707
Package NDCs from labels
13985-707-15
Manufacturer
MWI | Bimeda Inc. | Bimeda MTC Animal Health
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
Prevail - MWI | Bimeda Inc. | Bimeda MTC Animal HealthMWI | Bimeda Inc. | Bimeda MTC Animal Health2024-04-01PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13985-707-15Prevail30 g in 1 SYRINGEPASTE3012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13985-707PREVAIL (FLUNIXIN MEGLUMINE) PASTE [MWI]121 package rows20240402_f94b834f-e4c1-43ba-9463-5a8c249b4aec.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FLUNIXIN MEGLUMINEACTIVE INGREDIENT8Y3JK0JW3UPREVAIL (FLUNIXIN MEGLUMINE) PASTE [MWI]3
FLUNIXINACTIVE MOIETY356IB1O400PREVAIL (FLUNIXIN MEGLUMINE) PASTE [MWI]3

Reported adverse events (FAERS/openFDA)#

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