FDA.reportPublic FDA data

Flunixin Meglumine

Manufacturer
AX Pharmaceutical Corp
Effective date
2023-12-13
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
2
Source
full-release
Hydrated at
2026-06-01 02:50:58

Label at a glance#

ProductFlunixin Meglumine
Active ingredientFLUNIXIN MEGLUMINE
Label structure1 sections

Label contents#

Full prescribing information#

Flunixin Meglumine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-078-01Flunixin Meglumine0.5 kg in 1 JARPOWDER0.52
73377-078-02Flunixin Meglumine25 kg in 1 DRUMPOWDER252
73377-078-03Flunixin Meglumine20 kg in 1 DRUMPOWDER202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-078FLUNIXIN MEGLUMINE POWDER [AX PHARMACEUTICAL CORP]23 package rows20231214_b4a6aaa9-bcdd-44d9-b84d-92c99a51cd1d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73377-07873377-078-01, 73377-078-02, 73377-078-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
FLUNIXIN MEGLUMINE8Y3JK0JW3UACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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